SITE-SPECIFIC GENOME MODIFICATION TECHNOLOGY
h The present disclosure provides compositions, methods, and systems related to template-mediated genome editing and modification. In particular, the present disclosure provides novel genome modification technology involving site-specific chemical modification of a nucleotide to introduce a replication-blocking lesion. The compositions, methods, and systems described herein facilitate efficient site-specific genome modification of a DNA target, while minimizing the unintended edits and cellular toxicity associated with current genome editing approaches.
This application claims priority to and the benefit of U.S. Provisional Patent Application No. 63/149,419 filed Feb. 15, 2021, which is incorporated herein by reference in its entirety and for all purposes.
GOVERNMENT FUNDINGThis invention was made with government support under grant number GM119561 awarded by the National Institutes of Health. The government has certain rights in the invention.
SEQUENCE LISTINGThe text of the computer readable sequence listing filed herewith, titled “39212-601_SEQUENCE_LISTING_ST25”, created Feb. 14, 2022, having a file size of 144,908 bytes, is hereby incorporated by reference in its entirety.
FIELDThe present disclosure provides compositions, methods, and systems related to template-mediated genome modification. In particular, the present disclosure provides novel genome modification technology involving site-specific chemical modification of a nucleotide to introduce a replication-blocking lesion. The compositions, methods, and systems described herein facilitate efficient site-specific genome modification of a DNA target, while minimizing the unintended edits and cellular toxicity associated with current genome editing approaches.
BACKGROUNDCRISPR-based genome editing tools have found widespread application, relying on their easily programmable targeting and robust activity. Early use of these CRISPR-based tools has focused on the ability of Cas nucleases to cleave DNA. In the process of repairing the cleaved DNA, a genomic edit is introduced through homologous recombination with a supplied DNA repair template. DNA cleavage is, however, among the most toxic cellular events; DNA cleavage sets off cellular alarm systems which lead to mutations, DNA re-arrangements, or loss of cellular viability. Subsequent CRISPR-Cas genome editing tools have sought alternative approaches through target modification of individual bases or integration of a short template encoded within the guide RNA. Still, these methods are restricted in the range of edits that can be generated and can produce undesired edits. Therefore, there is a need for efficient genome editing and modification platforms that overcome the limitations of current systems.
SUMMARYEmbodiments of the present disclosure include a composition for targeted genome modification. In accordance with these embodiments, the composition includes a gap editor complex comprising a DNA-recognition domain and a DNA-modifying domain, wherein the DNA-recognition domain binds a DNA target sequence in the genome, and wherein the DNA-modifying domain induces formation of a replication blocking moiety on at least one nucleotide in the genome.
In some embodiments, the composition further comprises a donor nucleic acid template. In some embodiments, the donor nucleic acid template comprises a polynucleotide from an endogenous homologous sequence corresponding to the DNA target sequence. In some embodiments, the donor nucleic acid template comprise an exogenous single-stranded DNA (ssDNA) molecule or double-stranded DNA (dsDNA) molecule. In some embodiments, the donor nucleic acid template is an RNA molecule. In some embodiments, the presence of the donor nucleic acid template facilitates homology-directed gap repair and/or recombination, wherein the donor nucleic acid template or a fragment thereof is recombined into the genome of the DNA target sequence.
In some embodiments, the DNA-recognition domain comprises at least one Cas protein or fragment thereof lacking deoxyribonuclease activity. In some embodiments, the DNA-recognition domain comprises a complex of Cas proteins lacking deoxyribonuclease activity. In some embodiments, the DNA-recognition domain comprises a Cas protein or fragment thereof having nickase activity. In some embodiments, the Cas protein or Cas protein complex comprises a Type I Cascade, a Type II Cas9, a Type IV effector module, a Type V Cas12, a Cas9-related IscB, a Cas9-related TnpB, and combinations thereof.
In some embodiments, the DNA-recognition domain and the DNA-modifying domain are functionally coupled. In some embodiments, functionally coupled comprises polypeptide fusions, peptide tags, peptide linkers, RNA tags, and any combinations thereof.
In some embodiments, the DNA-modifying domain blocks DNA replication by adding the replication blocking moiety to: (i) at least one nucleotide in the DNA strand complementary to the DNA target sequence; (ii) at least one nucleotide in the DNA strand containing the DNA target sequence; or (iii) both at least one nucleotide in the DNA strand complementary to the DNA target sequence and at least one nucleotide in the DNA strand containing the DNA target sequence.
In some embodiments, the DNA-recognition domain induces a single-stranded break in the DNA target strand, and the DNA-modifying domain adds the replication blocking moiety to at least one nucleotide in the DNA strand complementary to the DNA target sequence.
In some embodiments, the DNA-modifying domain has been engineered to have reduced DNA binding, increased specificity to single-stranded DNA, and/or decreased enzymatic activity.
In some embodiments, the DNA-modifying domain catalyzes addition of ADP ribose to a thymine or guanine nucleotide. In some embodiments, the DNA-modifying domain comprises a DarT enzyme or a functional fragment, derivative, or variant thereof. In some embodiments, the DNA-modifying domain comprises a catalytic domain having at least 70% amino acid sequence identity with any of SEQ ID NOs: 18-21. In some embodiments, the DarT enzyme comprises one or more of the following amino acid substitutions: G49D, K56A, M86L, R92A, and/or R193A.
In some embodiments, the DNA-modifying domain comprises a Scabin enzyme or a functional fragment, derivative, or variant thereof. In some embodiments, the DNA-modifying domain comprises a catalytic domain having at least 70% amino acid sequence identity with any of SEQ ID NOs: 22-24. In some embodiments, the Scabin enzyme comprises an amino acid substitution that is K130A.
In some embodiments, the DNA-modifying domain catalyzes methylcarbamoylation of an adenine nucleotide. In some embodiments, the DNA-modifying domain comprises a Mom enzyme or a functional fragment, derivative, or variant thereof. In some embodiments, the DNA-modifying domain comprises a catalytic domain having at least 70% amino acid sequence identity with SEQ ID NO: 25-27. In some embodiments, the Mom enzyme comprises an amino acid substitution that is D149A.
In some embodiments, the DNA-modifying domain catalyzes addition a replication blocking moiety selected from the group consisting of: glucose, threonyl carbamoyl adenosine, acetate, glyceryl, L-ascorbic acid, uridine, adenosine mono-phosphate, a lipid, an amino acid, agmatine, L-threonylcarbamoyladenylate, L-threonylcarbamoyl, methylthiolate, sulfur, a methyl group, S-adenosyl-L-methione or a subgroup of S-adenosyl-L-methione, and dimethylallyl diphosphate or a subgroup thereof.
In some embodiments, the DNA-modifying enzyme domain comprises an enzyme or functional fragment, derivative, or variant thereof, selected from the group consisting of: Pierisin, Scabin, Cell cycle and apoptosis regulator 1 (CARP-1), SCO5461 protein (ScARP), adenine modification enzyme, acetyltransferase, amino acid transferase, nucleotidyl transferase, uridyltransferase, acyltransferase, ADP-ribsoyltransferase, methylthiotransferase, N-acetyl transferase 10, tRNA(Met) cytidine acetyltransferase (TmcA), tRNA cytidine acetyltransferase, GCN5-related N-acetyltransferase, lysidine synthase, m7G methyltransferase, N6 carbamoylmethyltransferase (Mom), N6-adenosine threonylcarbamoyltransferase, threonyl carbomyl transferase or threonyl carbomyl transferase complex, TsaB-TsaE-TsaD (TsaBDE) complex, tRNA N6-adenosine threonylcarbamoyltransferase (Qri7, Tcs4), methyltransferase, ATrm5a, tRNA:m1G/imG2 methyltransferase, tRNA (adenosine(37)-N6)-dimethylallyltransferase, tRNA dimethylallyltransferase (MiaA), and isopentenyltransferase.
In some embodiments, the composition comprises at least one guide RNA molecule. In some embodiments, the at least one guide RNA comprises gRNA, sgRNA, crRNA, or any combinations thereof. In some embodiments, the at least one guide RNA comprises a handle sequence and a targeting sequence. In some embodiments, the at least one guide RNA is complementary to the DNA target sequence.
In some embodiments, the composition further comprises at least one gap editor accessory factor. In some embodiments, the at least one gap editor accessory factor comprises a protein that augments at least one step in a genome modification process. In some embodiments, the at least one gap editor accessory factor is recruited to the gap editor complex via interaction with the DNA-modifying domain, the DNA-recognition domain, and/or the at least one guide RNA. In some embodiments, the recruitment of the at least one gap editor accessory factor to the gap editor complex comprises a peptide tag, a peptide linker, an RNA tag, and any combinations thereof. In some embodiments, the at least one gap editor accessory factor comprises Rap, DarG, Orf, ExoI, Exonuclease III, PrimPol, RecJ, RecQ1, Rad51, Rad52, CtIP, Rad18, and any combinations thereof.
Embodiments of the present disclosure also includes a kit for targeted genome modification. In accordance with these embodiments, the kit includes a gap editor complex comprising a DNA-recognition domain and a DNA-modifying domain, wherein the DNA-recognition domain binds a DNA target sequence in the genome, and wherein the DNA-modifying domain induces formation of a replication blocking moiety on at least one nucleotide in the genome.
In some embodiments, the kit further comprises a donor nucleic acid template. In some embodiments, the presence of the donor nucleic acid template facilitates homology-directed gap repair and/or recombination.
In some embodiments, the kit further comprises a guide RNA molecule.
In some embodiments of the kit, the DNA-recognition domain comprises at least one Cas protein or fragment thereof lacking deoxyribonuclease activity. In some embodiments, the DNA-recognition domain comprises at least one Cas protein or fragment thereof having nickase activity. In some embodiments, the Cas protein or Cas protein complex comprises a Type I Cascade, a Type II Cas9, a Type IV effector module, a Type V Cas12, a Cas9-related IscB, a Cas9-related TnpB, and combinations thereof.
In some embodiments of the kit, the DNA-recognition domain and the DNA-modifying domain are functionally coupled. In some embodiments, the DNA-recognition domain induces a single-stranded break in the DNA target strand, and wherein the DNA-modifying domain adds the replication blocking moiety to at least one nucleotide in the DNA strand complementary to the DNA target sequence.
In some embodiments of the kit, the DNA-modifying domain catalyzes addition of ADP ribose to a thymine or guanine nucleotide. In some embodiments, the DNA-modifying domain comprises a DarT enzyme or a functional fragment, derivative, or variant thereof. In some embodiments, the DNA-modifying domain comprises a Scabin enzyme or a functional fragment, derivative, or variant thereof. In some embodiments, the DarT enzyme has been engineered to have reduced DNA binding, increased specificity to single-stranded DNA, and/or decreased enzymatic activity.
In some embodiments of the kit, the DNA-modifying domain catalyzes methylcarbamoylation of an adenine nucleotide. In some embodiments, the DNA-modifying domain comprises a Mom enzyme or a functional fragment, derivative, or variant thereof. In some embodiments, the Mom enzyme has been engineered to have reduced DNA binding, increased specificity to single-stranded DNA, and/or decreased enzymatic activity.
In some embodiments of the kit, the DNA-modifying domain catalyzes addition a replication blocking moiety selected from the group consisting of: glucose, threonyl carbamoyl adenosine, acetate, glyceryl, L-ascorbic acid, uridine, adenosine mono-phosphate, a lipid, an amino acid, agmatine, L-threonylcarbamoyladenylate, L-threonylcarbamoyl, methylthiolate, sulfur, a methyl group, S-adenosyl-L-methione or a subgroup of S-adenosyl-L-methione, and dimethylallyl diphosphate or a subgroup thereof.
In some embodiments of the kit, the DNA-modifying enzyme domain comprises an enzyme or functional fragment, derivative, or variant thereof, selected from the group consisting of: Pierisin, Scabin, Cell cycle and apoptosis regulator 1 (CARP-1), SCO5461 protein (ScARP), adenine modification enzyme, acetyltransferase, amino acid transferase, nucleotidyl transferase, uridyltransferase, acyltransferase, ADP-ribsoyltransferase, methylthiotransferase, N-acetyl transferase 10, tRNA(Met) cytidine acetyltransferase (TmcA), tRNA cytidine acetyltransferase, GCN5-related N-acetyltransferase, lysidine synthase, m7G methyltransferase, N6 carbamoylmethyltransferase (Mom), N6-adenosine threonylcarbamoyltransferase, threonyl carbomyl transferase or threonyl carbomyl transferase complex, TsaB-TsaE-TsaD (TsaBDE) complex, tRNA N6-adenosine threonylcarbamoyltransferase (Qri7, Tcs4), methyltransferase, ATrm5a, tRNA:m1G/imG2 methyltransferase, tRNA (adenosine(37)-N6)-dimethylallyltransferase, tRNA dimethylallyltransferase (MiaA), and isopentenyltransferase.
In some embodiments of the kit, the at least one guide RNA comprises gRNA, sgRNA, crRNA, or any combinations thereof. In some embodiments, the at least one guide RNA comprises a handle sequence and a targeting sequence. In some embodiments, the targeting sequence in the at least one guide RNA is complementary to the DNA target sequence.
In some embodiments, the kit further comprises at least one gap editor accessory factor.
Embodiments of the present disclosure also include a method for targeted genome modification. In accordance with these embodiments, the method includes introducing any of the compositions of the present disclosure into a cell, and assessing the cell for presence of a desired genome alteration.
In some embodiments, a gap editor complex and/or a at least one guide RNA molecule are introduced into the cell as a polypeptide(s), mRNA(s), and/or DNA expression construct(s). In some embodiments, the gap editor complex and/or the guide RNA are introduced into the cell as part of a gene drive system.
In some embodiments, the cell is a prokaryotic cell or a eukaryotic cell. In some embodiments, the cell is a mammalian cell. In some embodiments, the cell is a plant cell.
In some embodiments, the method leads to a reduced degree of indel formation, chromosomal rearrangements, and/or DNA duplications.
In some embodiments, cell viability is enhanced and/or cell toxicity is reduced.
Other aspects and embodiments of the disclosure will be apparent in light of the following detailed description.
Nucleotide modifications can take the form of functional modifications, such as DNA methylation at certain positions, or damaging modification (DNA lesions), such as cross-linking, oxidation, and nitrosylation. These DNA lesions need to be repaired to maintain information fidelity and DNA functionality. Commonly occurring lesions are directly repaired through base excision, mismatch, and nucleotide excision repair processes. However, if these lesions are not repaired before DNA replication, then they can become locked into the genome as mutated DNA or stifle cellular division altogether. To avoid this, replication-dependent repair processes have evolved. One such process, translesion synthesis, can directly bypass some DNA lesions; however, this can introduce DNA mutations across some DNA lesions. Alternatively, replicating the DNA near the lesion can be skipped altogether by re-priming synthesis downstream of the lesion. This re-priming can occur via a lagging strand primase, or in higher eukaryotes by the leading strand primase-polymerase, PRIMPOL. This re-priming action enables replication to continue but leaves an unreplicated region complementary to the DNA lesion and surrounding DNA. The cell still needs to determine the appropriate sequence complementary to the DNA lesion, and to do this, cells employ a mechanism called homology-dependent gap repair (a subset of homologous recombination).
Homology-dependent gap repair (HDGR) is a highly accurate repair process in which a sister chromatid is used as a template to copy DNA complementary to the lesion-containing strand. As a subset of homologous recombination, experiments were conducted, as described further herein, to investigate whether this pathway could be co-opted to instead use an ectopic repair template instead of (or in addition to) the sister chromatid, generating synthetic genomic edits. Previous results demonstrated that site-specific introduction of abasic DNA could trigger HDGR and be completed using a plasmid-borne DNA template for repair, generating accurately edited genomic DNA. However, in some cases, this approach can be somewhat dependent on the stability of the abasic site. For example, an abasic site can be stabilized through inhibition of a cell's AP endonuclease activity but AP endonuclease inhibition can negatively affect cell viability and genomic stability and may not be feasible for some applications. Therefore, as described further herein, an alternative class of DNA lesions was identified that are not as susceptible to base excision or similar repair processes. Embodiments of the present disclosure include a class of lesions involving the addition of chemical groups to DNA that block DNA replication (replication blocking moiety) and facilitate HDGR.
For example, experiments were conducted to investigate whether the addition of adenosine-diphosphate ribose (ADPr) might be a promising DNA lesion candidate and act as a replication blocking moiety. ADPr transferases, which catalyze ADPr addition to nucleotides, are cytotoxic. Therefore, methods were developed to limit ADPr activity to the R-loop exposed after CRISPR-Cas binding to the genome, in an effort to trigger HDGR without loss of cell viability. Extracted dsDNA binding ADPr-transferases were shown to be lethal when electroporated into eukaryotic cells. Separately, dsDNA binding DNA modifying enzymes have been fused to DNA binding proteins to localize their activity, but they retain high rates of off-target modification, which necessitates additional mitigating steps to control activity. Single-stranded DNA binding enzymes can have their activity localized to the DNA R-loop exposed after target binding by a Cas effector to the DNA.
Previous work has described a class of single-stranded binding ADPr-transferase enzymes, including DarT and the DarT mutant DarT_G49D, which acts as a bacterial toxin. DarT expression is lethal in E. coli, and seems to be primarily repaired through recombination, and more weakly, through nucleotide excision repair. Therefore, experiments were conducted to investigate whether DarT could be used to trigger site-specific HDGR templated not by the genome, but by a recombinant DNA sequence. Experiments sought to understand whether DarT could be sufficiently controlled to localize ADPr modification to the Cas target site, avoiding cytotoxicity and allowing for efficient genome modification.
Section headings as used in this section and the entire disclosure herein are merely for organizational purposes and are not intended to be limiting.
1. DEFINITIONSUnless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art. In case of conflict, the present document, including definitions, will control. Preferred methods and materials are described below, although methods and materials similar or equivalent to those described herein can be used in practice or testing of the present disclosure. The phrase “in one embodiment” as used herein does not necessarily refer to the same embodiment, though it may. Furthermore, the phrase “in another embodiment” as used herein does not necessarily refer to a different embodiment, although it may. Thus, as described below, various embodiments of the invention may be readily combined, without departing from the scope or spirit of the invention. All publications, patent applications, patents and other references mentioned herein are incorporated by reference in their entirety. The materials, methods, and examples disclosed herein are illustrative only and not intended to be limiting.
The terms “comprise(s),” “include(s),” “having,” “has,” “can,” “contain(s),” and variants thereof, as used herein, are intended to be open-ended transitional phrases, terms, or words that do not preclude the possibility of additional acts or structures. The singular forms “a,” “and” and “the” include plural references unless the context clearly dictates otherwise. The present disclosure also contemplates other embodiments “comprising,” “consisting of” and “consisting essentially of,” the embodiments or elements presented herein, whether explicitly set forth or not.
For the recitation of numeric ranges herein, each intervening number there between with the same degree of precision is explicitly contemplated. For example, for the range of 6-9, the numbers 7 and 8 are contemplated in addition to 6 and 9, and for the range 6.0-7.0, the number 6.0, 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7, 6.8, 6.9, and 7.0 are explicitly contemplated.
“Correlated to” as used herein refers to compared to.
As used herein, the term “nucleic acid molecule” refers to any nucleic acid containing molecule, including but not limited to, DNA or RNA. The term encompasses sequences that include any of the known base analogs of DNA and RNA including, but not limited to, 4-acetylcytosine, 8-hydroxy-N6-methyladenosine, aziridinylcytosine, pseudoisocytosine, 5-(carboxyhydroxylmethyl) uracil, 5-fluorouracil, 5-bromouracil, 5-carboxymethylaminomethyl-2-thiouracil, 5-carboxymethylaminomethyluracil, dihydrouracil, inosine, N6-isopentenyladenine, 1-methyladenine, 1-methylpseudouracil, 1-methylguanine, 1-methylinosine, 2,2-dimethylguanine, 2-methyladenine, 2-methylguanine, 3-methylcytosine, 5-methylcytosine, N6-methyladenine, 7-methylguanine, 5-methylaminomethyluracil, 5-methoxyaminomethyl-2-thiouracil, beta-D-mannosylqueosine, 5′-methoxyc arbonylmethyluracil, 5-methoxyuracil, 2-methylthio-N6-isopentenyladenine, uracil-5-oxyacetic acid methylester, uracil-5-oxyacetic acid, oxybutoxosine, pseudouracil, queosine, 2-thiocytosine, 5-methyl-2-thiouracil, 2-thiouracil, 4-thiouracil, 5-methyluracil, N-uracil-5-oxyacetic acid methylester, uracil-5-oxyacetic acid, pseudouracil, queosine, 2-thiocytosine, and 2,6-diaminopurine.
The term “gene” refers to a nucleic acid (e.g., DNA) sequence that comprises coding sequences for the production of a polypeptide, precursor, or RNA (e.g., rRNA, tRNA, sRNA, microRNA, lincRNA). The polypeptide can be encoded by a full-length coding sequence or by any portion of the coding sequence so long as the desired activity or functional properties (e.g., enzymatic activity, ligand binding, signal transduction, immunogenicity, etc.) of the full-length or fragment are retained. The term also encompasses the coding region of a structural gene and the sequences located adjacent to the coding region on both the 5′ and 3′ ends for a distance of about 1 kb or more on either end such that the gene corresponds to the length of the full-length mRNA. Sequences located 5′ of the coding region and present on the mRNA are referred to as 5′ non-translated sequences. Sequences located 3′ or downstream of the coding region and present on the mRNA are referred to as 3′ non-translated sequences. The term “gene” encompasses both cDNA and genomic forms of a gene. A genomic form or clone of a gene contains the coding region interrupted with non-coding sequences termed “introns” or “intervening regions” or “intervening sequences.” Introns are segments of a gene that are transcribed into nuclear RNA (hnRNA); introns may contain regulatory elements such as enhancers. Introns are removed or “spliced out” from the nuclear or primary transcript; introns therefore are absent in the messenger RNA (mRNA) transcript. The mRNA functions during translation to specify the sequence or order of amino acids in a nascent polypeptide.
As used herein, the term “heterologous gene” refers to a gene that is not in its natural environment. For example, a heterologous gene includes a gene from one species introduced into another species. A heterologous gene also includes a gene native to an organism that has been altered in some way (e.g., mutated, added in multiple copies, linked to non-native regulatory sequences, etc.). Heterologous genes are distinguished from endogenous genes in that the heterologous gene sequences are typically joined to DNA sequences that are not found naturally associated with the gene sequences in the chromosome or are associated with portions of the chromosome not found in nature (e.g., genes expressed in loci where the gene is not normally expressed).
As used herein, the term “oligonucleotide,” refers to a short length of single-stranded polynucleotide chain. Oligonucleotides are typically less than about 300 residues long (e.g., between 15 and 100), however, as used herein, the term is also intended to encompass longer polynucleotide chains. Oligonucleotides are often referred to by their length. For example, a 24-residue oligonucleotide is referred to as a “24-mer.” Oligonucleotides can form secondary and tertiary structures by self-hybridizing or by hybridizing to other polynucleotides. Such structures can include, but are not limited to, duplexes, hairpins, cruciforms, bends, and triplexes.
The term “homology” and “homologous” refers to a degree of identity. There may be partial homology or complete homology. A partially homologous sequence is one that is less than 100% identical to another sequence.
As used herein, the terms “complementary” or “complementarity” are used in reference to polynucleotides (e.g., a sequence of nucleotides such as an oligonucleotide or a target nucleic acid) related by the base-pairing rules. For example, for the sequence “5′-A-G-T-3′” is complementary to the sequence “3′-T-C-A-5′.” Complementarity may be “partial,” in which only some of the nucleic acids' bases are matched according to the base pairing rules. Or, there may be “complete” or “total” complementarity between the nucleic acids. The degree of complementarity between nucleic acid strands has significant effects on the efficiency and strength of hybridization between nucleic acid strands. This is of particular importance in amplification reactions, as well as detection methods that depend upon binding between nucleic acids. Either term may also be used in reference to individual nucleotides, especially within the context of polynucleotides. For example, a particular nucleotide within an oligonucleotide may be noted for its complementarity, or lack thereof, to a nucleotide within another nucleic acid strand, in contrast or comparison to the complementarity between the rest of the oligonucleotide and the nucleic acid strand.
In some contexts, the term “complementarity” and related terms (e.g., “complementary”, “complement”) refers to the nucleotides of a nucleic acid sequence that can bind to another nucleic acid sequence through hydrogen bonds, e.g., nucleotides that are capable of base pairing, e.g., by Watson-Crick base pairing or other base pairing. Nucleotides that can form base pairs, e.g., that are complementary to one another, are the pairs: cytosine and guanine, thymine and adenine, adenine and uracil, and guanine and uracil. The percentage complementarity need not be calculated over the entire length of a nucleic acid sequence. The percentage of complementarity may be limited to a specific region of which the nucleic acid sequences that are base-paired, e.g., starting from a first base-paired nucleotide and ending at a last base-paired nucleotide. The complement of a nucleic acid sequence as used herein refers to an oligonucleotide which, when aligned with the nucleic acid sequence such that the 5′ end of one sequence is paired with the 3′ end of the other, is in “antiparallel association.” Certain bases not commonly found in natural nucleic acids may be included in the nucleic acids of the present invention and include, for example, inosine and 7-deazaguanine. Complementarity need not be perfect; stable duplexes may contain mismatched base pairs or unmatched bases. Those skilled in the art of nucleic acid technology can determine duplex stability empirically considering a number of variables including, for example, the length of the oligonucleotide, base composition and sequence of the oligonucleotide, ionic strength and incidence of mismatched base pairs.
Thus, in some embodiments, “complementary” refers to a first nucleobase sequence that is at least 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 97%, 98%, or 99% identical to the complement of a second nucleobase sequence over a region of 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, or more nucleobases, or that the two sequences hybridize under stringent hybridization conditions. “Fully complementary” means each nucleobase of a first nucleic acid is capable of pairing with each nucleobase at a corresponding position in a second nucleic acid. For example, in certain embodiments, an oligonucleotide wherein each nucleobase has complementarity to a nucleic acid has a nucleobase sequence that is identical to the complement of the nucleic acid over a region of 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, or more nucleobases.
As used herein, a “double-stranded nucleic acid” may be a portion of a nucleic acid, a region of a longer nucleic acid, or an entire nucleic acid. A “double-stranded nucleic acid” may be, e.g., without limitation, a double-stranded DNA, a double-stranded RNA, a double-stranded DNA/RNA hybrid, etc. A single-stranded nucleic acid having secondary structure (e.g., base-paired secondary structure) and/or higher order structure comprises a “double-stranded nucleic acid”. For example, triplex structures are considered to be “double-stranded”. In some embodiments, any base-paired nucleic acid is a “double-stranded nucleic acid”
The term “isolated” when used in relation to a nucleic acid, as in “an isolated oligonucleotide” or “isolated polynucleotide” refers to a nucleic acid sequence that is identified and separated from at least one component or contaminant with which it is ordinarily associated in its natural source. Isolated nucleic acid is such present in a form or setting that is different from that in which it is found in nature. In contrast, non-isolated nucleic acids as nucleic acids such as DNA and RNA found in the state they exist in nature. For example, a given DNA sequence (e.g., a gene) is found on the host cell chromosome in proximity to neighboring genes; RNA sequences, such as a specific mRNA sequence encoding a specific protein, are found in the cell as a mixture with numerous other mRNAs that encode a multitude of proteins. However, isolated nucleic acid encoding a given protein includes, by way of example, such nucleic acid in cells ordinarily expressing the given protein where the nucleic acid is in a chromosomal location different from that of natural cells, or is otherwise flanked by a different nucleic acid sequence than that found in nature. The isolated nucleic acid, oligonucleotide, or polynucleotide may be present in single-stranded or double-stranded form. When an isolated nucleic acid, oligonucleotide or polynucleotide is to be utilized to express a protein, the oligonucleotide or polynucleotide will contain at a minimum the sense or coding strand (i.e., the oligonucleotide or polynucleotide may be single-stranded), but may contain both the sense and anti-sense strands (i.e., the oligonucleotide or polynucleotide may be double-stranded).
As used herein, the term “purified” or “to purify” refers to the removal of components (e.g., contaminants) from a sample. For example, antibodies are purified by removal of contaminating non-immunoglobulin proteins; they are also purified by the removal of immunoglobulin that does not bind to the target molecule. The removal of non-immunoglobulin proteins and/or the removal of immunoglobulins that do not bind to the target molecule results in an increase in the percent of target-reactive immunoglobulins in the sample. In another example, recombinant polypeptides are expressed in bacterial host cells and the polypeptides are purified by the removal of host cell proteins; the percent of recombinant polypeptides is thereby increased in the sample.
Preferred methods and materials are described below, although methods and materials similar or equivalent to those described herein can be used in practice or testing of the present disclosure. All publications, patent applications, patents and other references mentioned herein are incorporated by reference in their entirety. The materials, methods, and examples disclosed herein are illustrative only and not intended to be limiting.
2. GAP EDITORSCRISPR-based genome editing tools have found widespread application, relying on their easily programmable targeting and robust activity. Early use of these CRISPR-based tools has focused on the ability of Cas nucleases to cleave DNA. In the process of repairing the cleaved DNA, a genomic edit is introduced. DNA cleavage is, however, among the most toxic events a cell can endure. DNA cleavage sets off cellular alarm systems which lead to mutations, DNA rearrangements, or loss of cellular viability. Subsequent CRISPR-Cas genome editing tools have sought to minimize these toxic effects by instead introducing single-stranded nicks or directly modifying DNA via an enzyme. Still, these newer methods exhibit a limited range of edits that can be introduced and can suffer from undesired insertions, deletions, and mutations.
Embodiments of the present disclosure demonstrate that efficient non-toxic genome modification can be performed through the introduction and repair of single-stranded DNA gaps. Previous work has demonstrated that site-specific introduction of abasic sites into DNA drives homology-dependent gap recombination. By introducing an ectopic DNA repair template, genome modification can be achieved at DNA sequences adjacent to the introduced abasic site. However, in some cases, this approach can be dependent on the stabilization of the abasic sites. Therefore, embodiments of the present disclosure include the development of a system to induce homology-dependent gap repair with the addition of stable chemical groups onto DNA. This modified DNA is not recognized or repaired by cellular glycosylases, which increases lesion stability, and drives homology-dependent gap repair. Site specific DNA targeting is achieved by fusion of the modification enzyme to a Cas effector, and in some cases, the rate of genome modification can be increased using a Cas effector to nick the target DNA strand. As described further herein, the combination of nicking and DNA modification can have synergistic effects on genome modification because they mutually abrogate sister chromatid repair.
As would be recognized by one of ordinary skill in the art, the original and most widely used CRISPR-Cas genome editing technology relies on Cas nucleases introducing a double strand break which is then repaired through homologous recombination via an editing template, similar to gap editors. While broadly applied, the toxicity of double-stranded breaks and their tendency to drive mutations or chromosomal rearrangements is a consistent challenge for therapeutic applications. These DNA breaks are highly toxic (particularly in bacteria) and often lead to error prone repair via non-homologous end joining pathways. Cleave and repair is potentially the best known way to insert large segments of DNA, which is important for many scientific and industrial applications.
Additionally, base editors can be used in an effort to avoid toxicity by enzymatically converting nucleotides from one to another. For example, cytosine can be converted to thymine and adenine can be converted to guanine. However, these base editors can only change one or a few nucleotides at a time, and they have to be carefully targeted to avoid undesired editing. Furthermore, base editors are mutagenic, meaning that untargeted nucleotides are more likely to be incorrectly replicated while the base editors are being used. Base editors are also constrained by the availability of target sequences. Compared to other techniques, base editors are relatively efficient and only rely on nicking a single strand of DNA, as opposed to cutting both strands.
Prime editors have only recently been described. Based on recent publications, it seems that prime editors are relatively efficient, and they have a major advantage in that they use a very small repair template which is encoded on the backbone of the Cas9 single guide RNA. While touted as a double-strand break-free technique, efficient prime editing still involves nicking both strands of DNA in relatively close (<200 bp) proximity This dual nicking is only moderately less toxic than the cleave-and-repair approach. Error-prone insertions and deletions still occur in mammalian cells as a result of dual nicking. It is unclear to what degree prime editors will function in prokaryotes. It also is unclear whether any mutagenic side effects might occur in their application, though their CRISPR-dependent off-target activity is muted.
As compared to other techniques, gap editors have the least amount of data pertaining to their use. Regardless, gap editors seem to have minimal toxic effects, as described further herein; and some experiments show no detectable toxicity. The lack of toxicity may be especially advantageous for therapeutic applications, as low toxicity typically indicates a low rate of undesired mutations, DNA insertions, or DNA rearrangements. Also, multiplex engineering is commonly hampered by toxicity (particularly in bacteria). For in vivo therapeutics, gap editors would likely suffer from the same DNA and protein delivery issues as all of the other CRISPR-Cas methods, although there are newer delivery platforms that allow co-delivery of RNPs with repair templates.
Embodiments of the present disclosure include compositions, systems, kits, and methods for targeted modification of a nucleic acid in a genome. In accordance with these embodiments, the present disclosure provides gap editors and gap editor complexes that generally include a DNA-recognition domain and a DNA-modifying domain. As described further in the Examples provided herein, gap editors and gap editor complexes facilitate programmable DNA targeting with a DNA-recognition domain that is functionally coupled to a DNA-modifying domain to drive genome modification via homology-directed gap repair. In some embodiments, the DNA-recognition domain binds a DNA target sequence in the genome, and the DNA-modifying domain induces formation of a replication blocking moiety on at least one nucleotide in the genome. Targeting of gap editors in a specific orientation generates persistent DNA gaps, thereby improving gap editor efficiency.
In some embodiments, the DNA-recognition domain and the DNA-modifying domain are functionally coupled. Functionally coupled includes any means for integrating the DNA-recognition domain and the DNA-modifying domain at a specific target site for the purposes of functioning as genome editors. In some embodiments, “functionally coupled,” includes but is not limited to polypeptide fusions, peptide tags, peptide linkers, RNA tags, and any combinations thereof. For example, a gap editor or gap editor complex can include a DNA-recognition domain that is fused to a DNA-modifying domain (e.g., a fusion polypeptide). The DNA-recognition domain of the gap editor fusion protein recognizes a specific site (e.g., nucleic acid sequence in a genome) in a target nucleic acid, and the DNA-modifying domain is then capable of modifying one or more nucleic acids in or around the target site to facilitate genome modification.
As would be recognized by one of ordinary skill in the art based on the present disclosure, the gap editor complexes described herein can be used to modify any part of a genome of an organism or cell. For example, the gap editor complexes of the present disclosure can be used to target a specific site in a genome to generate a desired site-specific modification, and/or the gap editor complexes of the present disclosure can be used to target one or more specific sites in a genome to generate a modification that results in the addition, exchange, and/or removal of a portion of the genome. Additionally, the gap editor complexes of the present disclosure can be used to target any region of a gene, including but not limited to, an open reading frame, an intron, an exon, an intron-exon boundary, a functional non-coding region, and any upstream and/or downstream DNA/gene regulatory sequences. The terms “DNA/gene regulatory sequences,” “control elements,” and “regulatory elements,” used interchangeably herein, refer to transcriptional and translational control sequences, such as promoters, enhancers, polyadenylation signals, terminators, protein degradation signals, and the like, that provide for and/or regulate transcription of a non-coding sequence or a coding sequence and/or regulate translation of an encoded polypeptide. Thus, the gap editor complexes of the present disclosure can be used to generate modifications in the genome that result in altered gene expression patterns and/or activity (e.g., upregulation or downregulation).
In some embodiments, the DNA-recognition domain and the DNA-modifying domain do not comprise a fusion polypeptide (e.g., do not form a single fusion polypeptide or protein). In some embodiments, the DNA-modifying domain is recruited to the gap editor or gap editor complex by the DNA-recognition domain. For example, the DNA-recognition domain of the gap editor can recruit the DNA-modifying domain via a protein-protein interaction. In some embodiments, this recruitment is facilitated by a tag or linker that serves to recruit and functionally couple the DNA-modifying domain to the DNA-recognition domain at a specific site of a target nucleic acid. Other means for recruiting and functionally coupling the DNA-modifying domain to the DNA-recognition domain based on protein-protein interactions can also be used, including but not limited to, antigen-antibody interactions (e.g., the DNA-modifying domain fused to an antigen binding domain and the DNA-recognition domain fused to the corresponding antigen), protein tags (e.g., a streptavidin-biotin interaction), a peptide and single chain variable antibody fragment, a split-protein system, or any ligand-receptor interaction. In other embodiments, the DNA-modification domain can be integrated into the DNA-recognition domain, such as, for example, by replacing the HNH domain of Cas9 with the DNA-modification domain, or inserting the DNA-modification domain into the PAM-interacting domain.
In other embodiments, the DNA-modifying domain is recruited to the gap editor or gap editor complex by an interaction with a nucleic acid. For example, a guide RNA molecule that interacts with the DNA-recognition domain to bind a site in a target nucleic acid can include a sequence and/or structure that binds the DNA-modifying domain (e.g., a scaffold domain) In some embodiments, the sequence and/or structure on the guide RNA includes domains that are recognized by RNA binding proteins. In some embodiments, the -modifying domain is fused to an RNA-binding protein that is recruited to the gap editor or gap editor complex via binding to the domain on the guide RNA. Other means for recruiting and functionally coupling the DNA-modifying domain to the DNA-recognition domain based on RNA-binding interactions can also be used. In some embodiments, the guide RNA is extended to encode an RNA aptamer that recognizes different proteins or protein domains, such as the MS2 coat protein, Tat, or Rev. The recognized protein or protein domain is then fused to the DNA-modifying domain. The guide RNA can encode multiple copies of the same protein-binding domain or different protein-binding domains. These protein-binding domains can be incorporated into different parts of the gRNA, such as through the loop of the gRNA or sgRNA or at the 3′ end of the sgRNA.
As described further herein, the gap editor complexes of the present disclosure can be used to generate various modifications in the genome of an organism or cell, such as through the mechanism of homology directed repair. In some embodiments, genome modifications using the gap editors of the present disclosure can generate specific nucleotide modifications ranging from a single nucleotide change to large insertions or deletions. In some embodiments, the gap editor complexes of the present disclosure can be used to add or remove large sequences of DNA through the use of more than one guide RNA sequence to target distinct sites in the genome (e.g., generate large genomic deletions by removing the sequence between two gRNA target sites and/or inserting an exogenous DNA sequence). In some embodiments, multiple gRNAs can be used to target multiple sites in a genome to generate any number of desired modifications in a genome (e.g., multiplexing). As would be recognized by one of ordinary skill in the art based on the present disclosure, any type of genetic modification can be achieved using the gap editor complexes of the present disclosure in any cell type and/or organism, regardless of how the gap editor complexes are delivered to the cell (e.g., transformation), including in vitro, ex vivo, or in vivo methods of delivery. A general discussion of these methods can be found in Ausubel, et al., Short Protocols in Molecular Biology, 3rd ed., Wiley & Sons, 1995.
DNA-Recognition Domains. In accordance with these embodiments, the DNA-recognition domains of the gap editors or gap editor complexes of the present disclosure include use of a sequence-specific nucleic acid binding component (e.g., molecule, biomolecule, or complex of one or more molecules and/or biomolecules) to target a specific nucleic acid target site). In some embodiments, the DNA-recognition domain includes at least one Cas protein or fragment thereof lacking nuclease or deoxyribonuclease activity. In some embodiments, the DNA-recognition domain comprises a complex of Cas proteins lacking nuclease or deoxyribonuclease activity. In some embodiments, the DNA-recognition domain includes at least one Cas protein or a complex of Cas proteins that exhibit nickase activity, including but not limited to, a Cas9 or a Cas12a with nickase activity.
In some embodiments, the Cas protein or Cas protein complex comprises a Type I Cascade, a Type II Cas9, a Type IV effector module, a Type V Cas12, a Cas9-related IscB, a Cas9-related TnpB, and combinations thereof. Cascade is a set of Cas proteins that form a stable complex in different proportions with the guide RNA. The gRNA is normally encoded within a CRISPR array, where the Cas6 protein of the complex cleaves a hairpin in the transcribed repeat. The other proteins then form around the freed RNA. The fully-formed complex binds target DNA flanked by a protospacer-adjacent motif (PAM) encoded on the 5′ end of the non-target strand. Upon target recognition, the complex then recruits the Type I endonuclease Cas3 to nick and processively degrade the non-target strand in the 3′-to-5′ direction, although the complex will stably bind target DNA in the absence of Cas3. The specific number and stoichiometry of the proteins in Cascade varies between CRISPR-Cas sub-types, such as Cas8c(1):Cas5c(1):Cas7(7) for the I-C sub-type and Cse1(1):Cse2(2):Cas5e(1):Cas7(6):Cas6e(1) for the I-E sub-type. Furthermore, these proteins can be fused to recapitulate the complex with fewer expressed polypeptides, and the Cas6 protein is dispensable if the guide RNA is expressed as a processed CRISPR RNA. Varying the length of the guide sequence within the gRNA can further alter the protein stoichiometry of Cascade and can change the length of the R-loop and displaced DNA strand. Cas9 is a single-effector nuclease that binds target DNA with a PAM encoded on the 3′ end of the non-target strand. Bound DNA is then nicked on opposite strands through the HNH and RuvC domains of Cas9, resulting in a double-stranded break. The gRNA utilized by Cas9 is normally encoded with a CRISPR array, where a trans-activating crRNA (tracrRNA) pairs with the transcribed repeat, and the RNA duplex is cleaved by the endoribonuclease RNase III. The resulting processed crRNA:tracrRNA duplex is bound by Cas9 and directs DNA targeting. The crRNA:tracrRNA duplex can be fused to form a single guide RNA (sgRNA). Cas12 represents a diverse family of Cas nucleases designated by their sub-type (e.g. Cas12a, Cas12e) and have been given alternative names such as Cpf1, C2c1, CasX, or Cas14a. Cas12 nucleases target DNA with a PAM encoded on the 5′ end of the non-target strand, with the nuclease's RuvC domain nicking the both the target and non-target stranded to create a staggered double-stranded break with a 5′ overhang. The gRNA is encoded within a CRISPR array and can be processed from the transcribed CRISPR array through one of two mechanisms depending on the nuclease: cleavage of a hairpin within the repeat by a riboendonucleolytic domain with the Cas12 nuclease (e.g. Cas12a), or pairing of the transcribed repeat with a tracrRNA that is subsequently cleaved by RNase III. As a result, the gRNA can be readily expressed in its processed form when the nuclease alone is responsible for crRNA processing, the gRNA can be expressed as an sgRNA when a tracrRNA is involved in crRNA processing.
In some embodiments, the DNA-recognition domain comprises a deoxyribonuclease-inactivated Cas9 (“dCas9”), which can be generated by introducing deactivating mutations within the HNH domain and the RuvC domain of the protein. In some embodiments, the DNA-recognition domain comprises a deoxyribonuclease-inactivated Cas12a (“dCas12a”), which can be generated by introducing deactivating mutations within at least one of the RuvC domains, such as RuvC-I. Alternatively, a guide RNA that is truncated on the PAM-distal end or contains mismatches with the target can allow DNA binding but not DNA nicking or cleavage by an otherwise catalytically active Cas nuclease.
In some embodiments, various other DNA-recognition domains can also be used in the gap editor complexes of the present disclosure. For example, certain embodiments of the compositions and methods described herein do not require guide RNAs to effectuate efficient genome editing and modification. As described above, these gap editor complexes include, but are not limited to, meganucleases, zinc-fingers (ZFs), and transcription activator-like effectors (TALEs). In some embodiments, the DNA-recognition domains of the present disclosure can include a meganuclease. Meganucleases can be used to replace, eliminate or modify sequences in a targeted manner and their recognition target sequence can be altered through protein engineering. Meganucleases can be used to modify all genome types, whether bacterial, plant or animal, and they are amendable to in vivo delivery due to their relatively small sizes. The high degree of target specificity of meganucleases allows for a concomitantly high degree of precision and much lower cell toxicity. However, targeting novel sequences is challenging due to the limited number of the meganuclease available.
In some embodiments, the DNA-recognition domains of the present disclosure can include zinc-fingers (ZFs). ZFs are fusions of the nonspecific DNA cleavage domain from the restriction endonuclease with zinc-finger proteins. ZFNs can target specific DNA sequences and this allows the ZFN to address and accurately change unique sequences inside a target organisms. A single zinc-finger is made up of around 30 amino acids in a conserved ββα figure. Some amino acids on the surface of the α-helix usually select three base pairs within the DNA smooth groove. Zinc-finger proteins have become an important framework for the design of custom DNA-binding proteins, as the development of unnatural arrays with more than three domains have become available, along with the development of a highly-conserved linker sequence that allows synthetic zinc-finger proteins, which recognize DNA sequences 9 to 18 bps in length.
In some embodiments, the DNA-recognition domains of the present disclosure can include transcription activator-like effectors (TALEs). TALES are very versatile and can be combined with numerous effector domains to affect genomic structure and function, including nucleases, transcriptional activators and repressors, recombinases, transposases, DNA and histone methyltransferases, and histone acetyltransferases. TALENs are transcription activator-like effector nucleases which are fusions of the Fokl cleavage domain and DNA-binding domains. TALEs are naturally occurring proteins from bacteria with genus Xanthomonas and contain DNA-binding domains made up of a series of 33-35 amino acid repeat domains that each recognize a single base pair. TALE specificity is determined by two hypervariable amino acids that are known as repeat-variable di-residues (RVDs). Numerous effector domains have been made available to fuse to TALE repeats for targeted genetic modifications, including nucleases, transcriptional activators, and site-specific recombinases. While the single base recognition of TALE-DNA binding repeats affords greater design flexibility than triplet-confined zinc-fingers, the cloning of repeat TALE arrays presents an elevated technical challenge due to extensive identical repeat sequences.
DNA-Modifying Domains. In some embodiments, the DNA-modifying domain catalyzes the formation or addition of at least one replication blocking moiety to at least one nucleotide in the DNA target sequence. In some embodiments, the DNA-modifying domain blocks DNA replication by adding the replication blocking moiety to at least one nucleotide in the DNA strand complementary to the DNA target sequence. In some embodiments, the DNA-modifying domain blocks DNA replication by adding the replication blocking moiety to at least one nucleotide in the DNA strand containing the DNA target sequence. In some embodiments, the DNA-modifying domain blocks DNA replication by adding the replication blocking moiety to both a nucleotide in the DNA strand complementary to the DNA target sequence and a nucleotide in the DNA strand containing the DNA target sequence.
In some embodiments, the DNA-recognition domain induces a single-stranded break in the DNA target strand (via nickase activity), and the DNA-modifying domain adds the replication blocking moiety to at least one nucleotide in the DNA strand complementary to the DNA target sequence. In some embodiments, the DNA-modifying domain catalyzes addition of ADP ribose to a thymine or guanine nucleotide. In some embodiments, the DNA-modifying domain comprises a DarT enzyme or a functional fragment, derivative, or variant thereof. In some embodiments, the DarT enzyme has been engineered to have reduced DNA binding, increased specificity to single-stranded DNA, and/or decreased enzymatic activity. DarT homologs (and any fragments, derivatives, or variants thereof) that can be used in the various embodiments disclosed herein include, but are not limited to, those provided in Table 1 below. In some embodiments, the DNA-modifying domain comprises a Scabin enzyme or a functional fragment, derivative, or variant thereof. In some embodiments, the Scabin enzyme has been engineered to have reduced DNA binding, increased specificity to single-stranded DNA, and/or decreased enzymatic activity. Scabin homologs (and any fragments, derivatives, or variants thereof) that can be used in the various embodiments disclosed herein include, but are not limited to, those provided in Table 1 below. In some embodiments, the Mom enzyme has been engineered to have reduced DNA binding, increased specificity to single-stranded DNA, and/or decreased enzymatic activity. Mom homologs (and any fragments, derivatives, or variants thereof) that can be used in the various embodiments disclosed herein include, but are not limited to, those provided in Table 1 below.
As would be recognized by one of ordinary skill in the art based on the present disclosure, other DNA-modifying domains/enzymes can be used in the gap editors and gap editor complexes of the present disclosure to induce formation of a replication blocking moiety at a given target site. For example, in some embodiments, the DNA-modifying domain/enzyme can include, but is not limited to, any of the following enzymes (or functional fragments, derivatives, or variants thereof): Pierisin, Scabin, Cell cycle and apoptosis regulator 1 (CARP-1), SCO5461 protein (ScARP), adenine modification enzyme, acetyltransferase, amino acid transferase, nucleotidyl transferase, uridyltransferase, acyltransferase, ADP-ribsoyltransferase, methylthiotransferase, N-acetyl transferase 10, tRNA(Met) cytidine acetyltransferase (TmcA), tRNA cytidine acetyltransferase, GCN5-related N-acetyltransferase, lysidine synthase, m7G methyltransferase, N6C carbamoylmethyltransferase (Mom), N6-adenosine threonylcarbamoyltransferase, threonyl carbomyl transferase or threonyl carbomyl transferase complex, TsaB-TsaE-TsaD (TsaBDE) complex, tRNA N6-adenosine threonylcarbamoyltransferase (Qri7, Tcs4), methyltransferase, ATrm5a, tRNA:m1G/imG2 methyltransferase, tRNA (adenosine(37)-N6)-dimethylallyltransferase, tRNA dimethylallyltransferase (MiaA), and isopentenyltransferase.
In some embodiments, the DNA-modifying domain used in the gap editor complexes of the present disclosure includes a catalytic domain (or a functional fragment, derivative, or variant thereof) that induces formation of a replication blocking moiety on at least one nucleotide in a genome. In some embodiments, the catalytic domain includes a portion of a DarT enzyme that is sufficient to carry out ADP-ribosylation of a target nucleic acid, as described further herein. In some embodiments, the catalytic domain includes a portion of a Scabin enzyme that is sufficient to carry out ADP-ribosylation of a target nucleic acid, as described further herein.
For example, the catalytic domain of the DNA-modifying domain that can be used in the gap editor complexes of the present disclosure includes, but is not limited to, any sequence having at least 70% amino acid identity with any of SEQ ID NOs: 18-21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 75% amino acid sequence identity with SEQ ID NO: 18. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 80% amino acid sequence identity with SEQ ID NO: 18. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 85% amino acid sequence identity with SEQ ID NO: 18. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 90% amino acid sequence identity with SEQ ID NO: 18. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 91% amino acid sequence identity with SEQ ID NO: 18. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 92% amino acid sequence identity with SEQ ID NO: 18. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 93% amino acid sequence identity with SEQ ID NO: 18. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 94% amino acid sequence identity with SEQ ID NO: 18. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 95% amino acid sequence identity with SEQ ID NO: 18. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 96% amino acid sequence identity with SEQ ID NO: 18. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 97% amino acid sequence identity with SEQ ID NO: 18. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 98% amino acid sequence identity with SEQ ID NO: 18. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 99% amino acid sequence identity with SEQ ID NO: 18.
In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 75% amino acid sequence identity with SEQ ID NO: 19. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 80% amino acid sequence identity with SEQ ID NO: 19. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 85% amino acid sequence identity with SEQ ID NO: 19. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 90% amino acid sequence identity with SEQ ID NO: 19. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 91% amino acid sequence identity with SEQ ID NO: 19. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 92% amino acid sequence identity with SEQ ID NO: 19. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 93% amino acid sequence identity with SEQ ID NO: 19. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 94% amino acid sequence identity with SEQ ID NO: 19. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 95% amino acid sequence identity with SEQ ID NO: 19. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 96% amino acid sequence identity with SEQ ID NO: 19. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 97% amino acid sequence identity with SEQ ID NO: 19. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 98% amino acid sequence identity with SEQ ID NO: 19. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 99% amino acid sequence identity with SEQ ID NO: 19.
In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 75% amino acid sequence identity with SEQ ID NO: 20. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 80% amino acid sequence identity with SEQ ID NO: 20. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 85% amino acid sequence identity with SEQ ID NO: 20. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 90% amino acid sequence identity with SEQ ID NO: 20. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 91% amino acid sequence identity with SEQ ID NO: 20. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 92% amino acid sequence identity with SEQ ID NO: 20. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 93% amino acid sequence identity with SEQ ID NO: 20. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 94% amino acid sequence identity with SEQ ID NO: 20. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 95% amino acid sequence identity with SEQ ID NO: 20. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 96% amino acid sequence identity with SEQ ID NO: 20. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 97% amino acid sequence identity with SEQ ID NO: 20. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 98% amino acid sequence identity with SEQ ID NO: 20. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 99% amino acid sequence identity with SEQ ID NO: 20.
In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 75% amino acid sequence identity with SEQ ID NO: 21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 80% amino acid sequence identity with SEQ ID NO: 21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 85% amino acid sequence identity with SEQ ID NO: 21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 90% amino acid sequence identity with SEQ ID NO: 21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 91% amino acid sequence identity with SEQ ID NO: 21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 92% amino acid sequence identity with SEQ ID NO: 21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 93% amino acid sequence identity with SEQ ID NO: 21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 94% amino acid sequence identity with SEQ ID NO: 21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 95% amino acid sequence identity with SEQ ID NO: 21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 96% amino acid sequence identity with SEQ ID NO: 21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 97% amino acid sequence identity with SEQ ID NO: 21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 98% amino acid sequence identity with SEQ ID NO: 21. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 99% amino acid sequence identity with SEQ ID NO: 21.
In some embodiments, the catalytic domain of the DNA-modifying domain that can be used in the gap editor complexes of the present disclosure includes, but is not limited to, any sequence having at least 70% amino acid identity with any of SEQ ID NOs: 22-24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 75% amino acid sequence identity with SEQ ID NO: 22. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 80% amino acid sequence identity with SEQ ID NO: 22. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 85% amino acid sequence identity with SEQ ID NO: 22. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 90% amino acid sequence identity with SEQ ID NO: 22. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 91% amino acid sequence identity with SEQ ID NO: 22. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 92% amino acid sequence identity with SEQ ID NO: 22. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 93% amino acid sequence identity with SEQ ID NO: 22. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 94% amino acid sequence identity with SEQ ID NO: 22. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 95% amino acid sequence identity with SEQ ID NO: 22. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 96% amino acid sequence identity with SEQ ID NO: 22. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 97% amino acid sequence identity with SEQ ID NO: 22. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 98% amino acid sequence identity with SEQ ID NO: 22. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 99% amino acid sequence identity with SEQ ID NO: 22.
In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 75% amino acid sequence identity with SEQ ID NO: 23. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 80% amino acid sequence identity with SEQ ID NO: 23. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 85% amino acid sequence identity with SEQ ID NO: 23. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 90% amino acid sequence identity with SEQ ID NO: 23. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 91% amino acid sequence identity with SEQ ID NO: 23. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 92% amino acid sequence identity with SEQ ID NO: 23. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 93% amino acid sequence identity with SEQ ID NO: 23. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 94% amino acid sequence identity with SEQ ID NO: 23. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 95% amino acid sequence identity with SEQ ID NO: 23. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 96% amino acid sequence identity with SEQ ID NO: 23. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 97% amino acid sequence identity with SEQ ID NO: 23. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 98% amino acid sequence identity with SEQ ID NO: 23. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 99% amino acid sequence identity with SEQ ID NO: 23.
In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 75% amino acid sequence identity with SEQ ID NO: 24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 80% amino acid sequence identity with SEQ ID NO: 24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 85% amino acid sequence identity with SEQ ID NO: 24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 90% amino acid sequence identity with SEQ ID NO: 24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 91% amino acid sequence identity with SEQ ID NO: 24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 92% amino acid sequence identity with SEQ ID NO: 24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 93% amino acid sequence identity with SEQ ID NO: 24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 94% amino acid sequence identity with SEQ ID NO: 24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 95% amino acid sequence identity with SEQ ID NO: 24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 96% amino acid sequence identity with SEQ ID NO: 24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 97% amino acid sequence identity with SEQ ID NO: 24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 98% amino acid sequence identity with SEQ ID NO: 24. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 99% amino acid sequence identity with SEQ ID NO: 24.
In some embodiments, the DNA-modifying domain used in the gap editor complexes of the present disclosure includes a catalytic domain (or a functional fragment, derivative, or variant thereof) of a Mom (also referred to as methylcarbamoyltransferase, methylcarbamoylase, or acetyltransferase). The catalytic domain can include the portion of a methylcarbamoylase enzyme that is sufficient to carry out methylcarbamoylation of adenine using acetyl CoA as a donor substrate transferred to a target nucleic acid, as described further herein. For example, the catalytic domain of a Mom that can be used as the DNA-modifying domain in the gap editor complexes of the present disclosure includes, but is not limited to, any sequence that has at least 70% amino acid identity with any of SEQ ID NOs: 25-27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 75% amino acid sequence identity with SEQ ID NO: 25. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 80% amino acid sequence identity with SEQ ID NO: 25. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 85% amino acid sequence identity with SEQ ID NO: 25. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 90% amino acid sequence identity with SEQ ID NO: 25. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 91% amino acid sequence identity with SEQ ID NO: 25. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 92% amino acid sequence identity with SEQ ID NO: 25. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 93% amino acid sequence identity with SEQ ID NO: 25. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 94% amino acid sequence identity with SEQ ID NO: 25. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 95% amino acid sequence identity with SEQ ID NO: 25. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 96% amino acid sequence identity with SEQ ID NO: 25. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 97% amino acid sequence identity with SEQ ID NO: 25. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 98% amino acid sequence identity with SEQ ID NO: 25. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 99% amino acid sequence identity with SEQ ID NO: 25.
In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 75% amino acid sequence identity with SEQ ID NO: 26. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 80% amino acid sequence identity with SEQ ID NO: 26. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 85% amino acid sequence identity with SEQ ID NO: 26. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 90% amino acid sequence identity with SEQ ID NO: 26. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 91% amino acid sequence identity with SEQ ID NO: 26. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 92% amino acid sequence identity with SEQ ID NO: 26. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 93% amino acid sequence identity with SEQ ID NO: 26. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 94% amino acid sequence identity with SEQ ID NO: 26. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 95% amino acid sequence identity with SEQ ID NO: 26. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 96% amino acid sequence identity with SEQ ID NO: 26. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 97% amino acid sequence identity with SEQ ID NO: 26. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 98% amino acid sequence identity with SEQ ID NO: 26. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 99% amino acid sequence identity with SEQ ID NO: 26.
In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 75% amino acid sequence identity with SEQ ID NO: 27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 80% amino acid sequence identity with SEQ ID NO: 27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 85% amino acid sequence identity with SEQ ID NO: 27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 90% amino acid sequence identity with SEQ ID NO: 27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 91% amino acid sequence identity with SEQ ID NO: 27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 92% amino acid sequence identity with SEQ ID NO: 27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 93% amino acid sequence identity with SEQ ID NO: 27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 94% amino acid sequence identity with SEQ ID NO: 27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 95% amino acid sequence identity with SEQ ID NO: 27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 96% amino acid sequence identity with SEQ ID NO: 27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 97% amino acid sequence identity with SEQ ID NO: 27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 98% amino acid sequence identity with SEQ ID NO: 27. In some embodiments, the DNA-modifying domain includes a catalytic domain having at least 99% amino acid sequence identity with SEQ ID NO: 27.
Replication Blocking Moieties. One of ordinary skill in the art would recognize, based on the present disclosure, that a replication blocking moiety can include, but is not limited to, glucose, threonyl carbamoyl adenosine, acetate, glyceryl, L-ascorbic acid, uridine, adenosine mono-phosphate, adenosine di-phosphate ribose, methylcarbamoyl, a lipid, an amino acid, agmatine, L-threonylcarbamoyladenylate, L-threonylcarbamoyl, methylthiolate, sulfur, a methyl group, S-adenosyl-L-methione or a subgroup of S-adenosyl-L-methione, and dimethylallyl diphosphate or a subgroup thereof. These and other replication blocking moieties have the general feature of being able to functionalize a nucleotide in a target sequence such that DNA replication is blocked and homology-directed gap repair is induced. This can occur by enzymatic means or by enzyme-independent means.
Guide RNA. Embodiments of the present disclosure also include gap editors and gap editor complexes that can include at least one guide RNA molecule. In accordance with these embodiments, the guide RNA molecule comprises a handle sequence and a targeting sequence. The targeting sequence interacts with a sequence in the target nucleic acid, and the handle sequence facilitates binding of the gap editor or gap editor complex. As would be recognized by one of ordinary skill in the art based on the present disclosure, a single chimeric guide RNA (sgRNA) can mimic the structure of an annealed crRNA/tracrRNA; this type of guide RNA has become more widely used than crRNA/tracrRNA because the gRNA approach provides a simplified system with only two components (e.g., the Cas9 and the sgRNA). Thus, sequence-specific binding to a nucleic acid target can be guided by a natural dual-RNA complex (e.g., comprising a crRNA, a tracrRNA, and Cas9) or a chimeric single-guide RNA (e.g., a sgRNA and Cas9). (see, e.g., Jinek et al. (2012) “A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity” Science 337:816-821). Multiple gRNAs can be further expressed using CRISPR arrays that naturally encode the crRNA utilized by the nucleases. The gRNAs can also be expressed separately by being operably linked to a promoter and terminator. The gRNAs can also be fused in a single transcript by including intervening RNA cleavages sites, such as ribozymes or sites recognized by RNA-cleaving enzymes such as RNase P, RNase Z, RNase III, or Csy4. The gRNAs or sgRNAs may include RNA templates for reverse transcription into cDNA repair templates. The sgRNAs may include aptamer sequences, for example, RNA-binding protein recognition sites so as to recruit accessory genome editing factors to the gap editor complex or gap editor target site.
As described further herein, genome modifications using the gap editors of the present disclosure can generate specific nucleotide modifications ranging from a single nucleotide change to large insertions or deletions. In some embodiments, the gap editor complexes of the present disclosure can be used to add, exchange, and/or remove large sequences of DNA through the use of more than one guide RNA sequence to target distinct sites in the genome. For example, large genomic deletions can be generated by removing the sequence between two gRNA target sites and/or inserting an exogenous DNA sequence (e.g., by virtue of the endogenous repair/recombination mechanisms in a cell or organism). In some embodiments, multiple gRNAs can be used to target multiple sites in a genome to generate any number of desired modifications in a genome (e.g., multiplexing).
In some embodiments, guide RNA molecules are not required in the gap editor complexes of the present disclosure. For example, certain embodiments of the compositions and methods described herein do not require guide RNAs to effectuate efficient genome editing and modification. As described above, these gap editor complexes include, but are not limited to, meganucleases, zinc-fingers (ZFs), and transcription activator-like effectors (TALEs).
Donor Template. In some embodiments, the presence of a donor nucleic acid template facilitates homology-directed gap recombination and/or repair, which includes the donor nucleic acid template or a fragment thereof being recombined into the double-stranded target DNA molecule. In some embodiments, the donor DNA template can serve as a replication template, resulting in the sequence encoded by the exogenous DNA or RNA being copied into the genome, but the exogenous DNA or RNA polynucleotide molecule itself is not directly transferred into the genome. The donor nucleic acid template can be single-stranded or double-stranded. In some embodiments, the donor template is a cDNA that has reversed transcribed from an endogenous, expressed, synthetic, or delivered RNA. The donor nucleic acid may be delivered into a cell as plasmid or linear DNA. A donor nucleic acid may also be generated in vivo from a template ribonucleic acid by a reverse transcriptase. In other embodiments, the donor nucleic acid may itself be a ribonucleic acid. The donor nucleic acid can also contain chemical modifications. The donor nucleic acid may include chemical modifications or sequences specifically recruited to the gap editor complex, or gap editor target site.
In some embodiments, the donor nucleic acid template comprises a polynucleotide from an endogenous homologous sequence corresponding to the DNA target sequence. In some embodiments, the donor nucleic acid template comprises a polynucleotide from an endogenous allele (e.g., to facilitate loss of heterozygosity). In some embodiments, the donor nucleic acid template comprise an exogenous single-stranded DNA (ssDNA) molecule or double-stranded DNA (dsDNA) molecule. In some embodiments, the presence of the donor nucleic acid template facilitates homology-directed gap repair and/or recombination, wherein the donor nucleic acid template or a fragment thereof is recombined into the genome of the DNA target sequence. In accordance with these embodiments, the gap editors of the present disclosure can be particularly advantageous for inserting large donor DNA sequences, replacing large segments of DNA, and/or removing large DNA sequences in a genome. In some embodiments, the gap editor complexes of the present disclosure can be used to add, exchange, and/or remove large sequences of DNA through the use of more than one guide RNA sequence to target distinct sites in the genome. For example, large genomic deletions can be generated by removing the sequence between two gRNA target sites and/or inserting an exogenous DNA sequence (e.g., by virtue of the endogenous repair/recombination mechanisms in a cell or organism). In some embodiments, multiple gRNAs can be used to target multiple sites in a genome to generate any number of desired modifications in a genome (e.g., multiplexing).
Accessory Factors. In some embodiments, the compositions and systems of the present disclosure further comprise a one gap editor accessory factor. In some embodiments, the composition further comprises at least one gap editor accessory factor. In some embodiments, the at least one gap editor accessory factor comprises a protein that augments at least one step in a genome modification process. In some embodiments, the at least one gap editor accessory factor is recruited to the gap editor complex via interaction with the DNA-modifying domain, the DNA-recognition domain, and/or the at least one guide RNA. In some embodiments, the recruitment of the at least one gap editor accessory factor to the gap editor complex comprises a peptide tag, a peptide linker, an RNA tag, and any combinations thereof. In some embodiments, the at least one gap editor accessory factor comprises Rap, DarG, Orf, ExoI, Exonuclease III, PrimPol, RecJ, RecQ1, Rad51, Rad52, CtIP, Rad18, and any combinations thereof. In some embodiments, and as described further herein, the present disclosure can include gap editor complexes in which the DNA-modifying domain comprises DarT. In accordance with these embodiments, DarG, TARG1, or another glycohydolase domain can be included as a gap editor accessory factor by modulating off-target editing (e.g., attenuating DarT activity) or removing the added ADPr after HDGR occurs.
As would be recognized by one of ordinary skill in the art based on the present disclosure, methods for delivering gap editors and gap editor complexes into a cell include any currently known methods and systems for delivering polynucleotides and/or polypeptides/proteins. For example, gap editors and gap editor complexes can be delivered using plasmid DNA, ssDNA, RNA, or other means for delivering polynucleotide molecules, including but not limited to, lipid-based delivery systems (e.g., using cationic lipids), conjugation from a donor cell, viral/bacteriophage-based delivery systems, and chemical-based systems (e.g., calcium phosphate precipitation, DEAE-dextran, polybrene). In some embodiments, the delivery system can include mechanical and/or electrical devices and methods for delivering the gap editors and gap editor complexes of the present disclosure as polynucleotides and/or as polypeptides/proteins (or any combinations thereof). In some embodiments, gap editors and gap editor complexes are delivered using a gene gun (e.g., bombardment and Agrobacterium transformation as used for plant cells), and electroporation-based methods, as well as any other physical methods (e.g., mechanical, electrical, thermal, optical, chemical stimulation, and the like) that use membrane disruption as a means for delivering polynucleotides and polypeptides/proteins (see, e.g., Sun et al., Recent advances in micro/nanoscale intracellular delivery, Nanotechnology and Precision Engineering 3, 18 (2020)).
3. KITS, SYSTEMS, AND METHODSEmbodiments of the present disclosure also include kits and systems for targeted modification of a nucleic acid. In accordance with these embodiments, the kit includes a gap editor complex comprising a DNA-recognition domain and a DNA-modifying domain. In some embodiments, the kit also includes at least one guide RNA molecule. In some embodiments, the DNA-recognition domain binds a DNA target sequence in the genome, and the DNA-modifying domain induces formation of a replication blocking moiety on at least one nucleotide in the genome. As would be recognized by one of ordinary skill based on the present disclosure, the kits and systems can also include one or more of the other components of the gene modification compositions described herein (e.g., gap editor accessory factors). In some embodiments of the kit, the composition further comprises a donor nucleic acid template. In some embodiments of the kit, the presence of the donor nucleic acid template facilitates homology-directed gap repair and/or recombination.
In some embodiments of the kit, the DNA-recognition domain comprises at least one Cas protein or fragment thereof lacking deoxyribonuclease activity. In some embodiments of the kit, the DNA-recognition domain comprises at least one Cas protein or fragment thereof having nickase activity. In some embodiments, the Cas protein or Cas protein complex comprises a Type I Cascade, a Type II Cas9, a Type IV effector module, a Type V Cas12, a Cas9-related IscB, a Cas9-related TnpB, and combinations thereof.
In some embodiments of the kit, the DNA-recognition domain and the DNA-modifying domain are functionally coupled. In some embodiments of the kit, the DNA-recognition domain induces a single-stranded break in the DNA target strand, and the DNA-modifying domain adds the replication blocking moiety to at least one nucleotide in the DNA strand complementary to the DNA target sequence. In some embodiments of the kit, the DNA-modifying domain catalyzes addition of ADP ribose to a thymine or guanine nucleotide. In some embodiments, the DNA-modifying domain comprises a DarT enzyme or a functional fragment, derivative, or variant thereof. In some embodiments of the kit, the DarT enzyme has been engineered to have reduced DNA binding, increased specificity to single-stranded DNA, and/or decreased enzymatic activity.
In some embodiments of the kit, the DNA-modifying domain catalyzes addition of a replication blocking moiety selected from the group consisting of: glucose, threonyl carbamoyl adenosine, acetate, glyceryl, L-ascorbic acid, uridine, adenosine mono-phosphate, a lipid, an amino acid, agmatine, L-threonylcarbamoyladenylate, L-threonylcarbamoyl, methylthiolate, sulfur, a methyl group, S-adenosyl-L-methione or a subgroup of S-adenosyl-L-methione, and dimethylallyl diphosphate or a subgroup thereof. In some embodiments of the kit, the DNA-modifying enzyme domain comprises an enzyme or functional fragment, derivative, or variant thereof, selected from the group consisting of: Pierisin, Scabin, Cell cycle and apoptosis regulator 1 (CARP-1), SCO5461 protein (ScARP), adenine modification enzyme, acetyltransferase, amino acid transferase, nucleotidyl transferase, uridyltransferase, acyltransferase, ADP-ribsoyltransferase, methylthiotransferase, N-acetyl transferase 10, tRNA(Met) cytidine acetyltransferase (TmcA), tRNA cytidine acetyltransferase, GCN5-related N-acetyltransferase, lysidine synthase, m7G methyltransferase, N6 carbamoylmethyltransferase (Mom), N6-adenosine threonylcarbamoyltransferase, threonyl carbomyl transferase or threonyl carbomyl transferase complex, TsaB-TsaE-TsaD (TsaBDE) complex, tRNA N6-adenosine threonylcarbamoyltransferase (Qri7, Tcs4), methyltransferase, ATrm5a, tRNA:m1G/imG2 methyltransferase, tRNA (adenosine(37)-N6)-dimethylallyltransferase, tRNA dimethylallyltransferase (MiaA), and isopentenyltransferase.
In some embodiments of the kit, the at least one guide RNA comprises gRNA, sgRNA, crRNA, or any combinations thereof. In some embodiments of the kit, the at least one guide RNA comprises a handle sequence and a targeting sequence. In some embodiments of the kit, the targeting sequence in the at least one guide RNA is complementary to the DNA target sequence. In some embodiments, the gap editor complexes of the present disclosure can be used to add, exchange, and/or remove large sequences of DNA through the use of more than one guide RNA sequence to target distinct sites in the genome. For example, large genomic deletions can be generated by removing the sequence between two gRNA target sites and/or inserting an exogenous DNA sequence (e.g., by virtue of the endogenous repair/recombination mechanisms in a cell or organism). In some embodiments, multiple gRNAs can be used to target multiple sites in a genome to generate any number of desired modifications in a genome (e.g., multiplexing).
Embodiments of the present disclosure also include methods for targeted modification of a nucleic acid. In accordance with these embodiments, the methods include introducing any of the components of the genome modification compositions described herein, and assessing the cell for presence of a desired genetic alteration using techniques known in the art. In some embodiments of the method, the components include gap editors and gap editor complexes comprising a DNA-recognition domain and a DNA-modifying domain, at least one guide RNA molecule, and a donor nucleic acid template. In some embodiments, one or more gap editor accessory factors can also be included. One or more of these factors can be introduced into a cell or organism as a polypeptide(s), mRNA(s), and/or DNA expression construct(s), or any combination thereof, by means known in the art. As would be recognized by one of ordinary skill in the art based on the present disclosure, the gap editor compositions, systems, and methods can be used to facilitate the modification of whole organisms, including but not limited to, humans, plants, livestock, and the like.
In some embodiments of the method, at least one of these components are introduced into the cell as part of a gene drive system. In a gene drive system, all or some of genome modification components such as the DNA-recognition domain, DNA-modifying domain, gRNA, and accessory factors are encoded within the donor nucleic acid sequence present in one copy of a chromosome. The gRNA directs the DNA-modifying domain to the sister chromosome in the region where the donor nucleic acid sequence would reside. Upon targeting by the gap editor proteins or complexes, the donor nucleic acid (which also encodes the gap editor system) is copied over to a new chromosome. Thus, the gap editor system becomes self-propagating, efficiently forming homozygously edited organisms. Example organisms in which gene drives can be implemented include fungi, flatworms, mosquitos, and mice.
In some embodiments, the compositions, systems, and methods of the present disclosure include one or more components that enhance or improve one or more aspects of gene modification. In some embodiments, improving or enhancing one or more aspects of genome modification includes the use of a gap editor accessory factor(s), as described above. In some embodiments, methods that enhance or improve one or more aspects of genome modification include reducing or attenuating nuclease activity in a cell in which genome modification is desired. Reducing nuclease activity in a cell can lead to enhanced or improved modification frequency and/or efficiency. In some embodiments, reducing nuclease activity in a cell includes reducing activity of an endogenous AP endonuclease (e.g., encoded by xthA) by any means known in the art. In some embodiments, nuclease activity in a cell can be reduced via genetic means and/or by pharmacological means (e.g., treatment with endonuclease inhibitors including but not limited to AJAY-4, CRT0044876, aurintricarboxylic acid, 6-hydroxy-DL-DOPA, Reactive Blue 2, myricetin, mitoxantrone, methyl-3,4-dephostatin, thiolactomycin, and (2E)-3-[5-(2,3-dimethoxy-6-methyl-1,4-benzoquinoyl)]-2-nonyl-2-propenoic acid (E3330)).
Embodiments of the compositions, systems, and methods provided herein can be used to edit the genome of a cell. The cell can be a prokaryotic cell, a eukaryotic cell, or a plant cell. In some embodiments, the cell is a mammalian cell. The present disclosure also provides an isolated cell comprising any of the components or systems described herein. Exemplary cells can include those that can be easily and reliably grown, have reasonably fast growth rates, have well characterized expression systems, and can be transformed or transfected easily and efficiently. Examples of suitable prokaryotic cells include, but are not limited to, cells from the genera Bacillus (such as Bacillus subtilis and Bacillus brevis), Clostridia (such as Clostridium difficile or Clostridium autoethanogenum), Escherichia (such as E. coli), Lactobacilli, Klebsiella, Myxobacteria, Pseudomonas, Streptomyces, Salmonella, Vibrio (such as Vibrio cholerae or Vibrio nutrifaciens) and Envinia. Suitable eukaryotic cells are known in the art and include, for example, yeast cells, insect cells, and mammalian cells. Examples of suitable yeast cells include those from the genera Kluyveromyces, Pichia, Rhino-sporidium, Saccharomyces, and Schizosaccharomyces. Exemplary insect cells include Sf-9 and HIS (Invitrogen, Carlsbad, Calif.) and are described in, for example, Kitts et al., Biotechniques, 14: 810-817 (1993); Lucklow, Curr. Opin. Biotechnol., 4: 564-572 (1993); and Lucklow et al., J. Virol., 67: 4566-4579 (1993).
In some embodiments, the compositions and methods of the present disclosure can be employed to induce DNA modification, and/or transcriptional modulation in mitotic or post-mitotic cells in vivo and/or ex vivo and/or in vitro (e.g., to produce genetically modified cells that can be reintroduced into an individual). Because the gap editors of the present disclosure include site-specific DNA-targeting, a mitotic and/or post-mitotic cell-of-interest can include a cell from any organism (e.g. a bacterial cell, an archaeal cell, a cell of a single-cell eukaryotic organism, a plant cell, an algal cell, e.g., Botryococcus braunii, Chlamydomonas reinhardtii, Nannochloropsis gaditana, Chlorella pyrenoidosa, Sargassum patens C. Agardh, and the like, a fungal cell (e.g., a yeast cell), an animal cell, a cell from an invertebrate animal (e.g. fruit fly, cnidarian, echinoderm, nematode, etc.), a cell from a vertebrate animal (e.g., fish, amphibian, reptile, bird, mammal), a cell from a mammal, a cell from a rodent, a cell from a human, etc.). Any type of cell may be of interest (e.g. a stem cell, e.g. an embryonic stem (ES) cell, an induced pluripotent stem (iPS) cell, a germ cell; a somatic cell, e.g. a fibroblast, a hematopoietic cell, a neuron, a muscle cell, a bone cell, a hepatocyte, a pancreatic cell; an in vitro or in vivo embryonic cell of an embryo at any stage, e.g., a 1-cell, 2-cell, 4-cell, 8-cell, etc. stage zebrafish embryo; etc.). Cells may be from established cell lines or they may be primary cells, where “primary cells”, “primary cell lines”, and “primary cultures” are used interchangeably herein to refer to cells and cells cultures that have been derived from a subject and allowed to grow in vitro for a limited number of passages of the culture. Target cells can include any unicellular organisms, multicellular organisms, or any cells grown in culture.
In some embodiments, the cell can also be a cell that is used for therapeutic purposes. The cell can be a mammalian cell, and in some embodiments, the cell is a human cell. A number of suitable mammalian and human cells are known in the art, and many are available from the American Type Culture Collection (ATCC, Manassas, Va.). Examples of suitable mammalian cells include, but are not limited to, Chinese hamster ovary cells (CHO) (ATCC No. CCL61), CHO DHFR-cells (Urlaub et al., Proc. Natl. Acad. Sci. USA, 97: 4216-4220 (1980)), human embryonic kidney (HEK) 293 or 293T cells (ATCC No. CRL1573), and 3T3 cells (ATCC No. CCL92). Other suitable mammalian cell lines are the monkey COS-1 (ATCC No. CRL1650) and COS-7 cell lines (ATCC No. CRL1651), as well as the CV-1 cell line (ATCC No. CCL70). Further exemplary mammalian cells include primate, rodent, and human cell lines, including transformed cell lines. Normal diploid cells, cell strains derived from in vitro culture of primary tissue, as well as primary explants, are also suitable. Other suitable mammalian cell lines include, but are not limited to, mouse neuroblastoma N2A cells, HeLa, HEK, A549, HepG2, mouse L-929 cells, and BHK or HaK hamster cell lines. Methods for selecting suitable cells and methods for transformation, culture, amplification, screening, and purification of cells are known in the art. Examples of suitable plant cell lines are derived from plants such as Arabidopsis (such as the Landsberg erecta cell line), sugarcane, tomato, pea, rice, wheat, tobacco (such as the BY-2 cell line).
In accordance with the methods described above embodiments, the compositions and systems of the present disclosure can be used to edit a genome of a cell in a manner that reduces the degree of indel formation, chromosomal rearrangements, or DNA duplications. In some embodiments, the compositions, systems, and methods described herein reduce cell toxicity as compared to currently available methods, at least in part due to the lack double-stranded breaks in the target nucleic acid.
4. MATERIALS AND METHODSMeasurement of gap editing in E. coli by a colorimetric assay was performed by co-transforming the DNA modifying domain fused to a DNA binding domain such as Cas9 (e.g. DarT-ScdCas9) and an sgRNA and nucleic acid donor into E. coli by electroporation and plated on LB agar plus the appropriate antibiotic(s). The resulting colonies were picked and inoculated into 750 mL of liquid LB media in a deep well plate shaking at 900 rpm and 37° C. for 12 to 16 hours overnight. Gap editor expression was induced by diluting overnight culture 1:500 into 750 mL of liquid LB media with antibiotics, 1 mM IPTG and 33 mM arabinose, shaking at 900 rpm for 8 hours. After 8 hours, samples were removed for spot plating on LB agar with antibiotics, IPTG, and X-gal. The next day, white and blue colonies were counted to determine frequency of lacZ recombination and repair. Repair was confirmed by sanger sequencing.
Measurement of gap editing in E. coli by antibiotic resistance assays was performed by co-transforming a DNA modifying domain fused to a DNA binding domain such as Cas9 or Cas12a, and an sgRNA with nucleic acid donor by electroporation. The transformation mixture was plated on LB agar plus the appropriate antibiotics. The resulting colonies were picked and inoculated into 750 mL of liquid LB media in a deep well plate shaking at 900 rpm and 30° C. for 12 to 16 hours overnight. Gap editor cultures were first back-diluted 1:100 into liquid LB with antibiotics shaking at 37° C. for 1 hour. Gap editor expression was then induced by further diluting this culture 1:100 into 750 mL of liquid LB media with antibiotics and 33 mM arabinose, shaking at 900 rpm for 5 hours. After 5 hours of induction, samples were removed for spot plating on two separate LB agar plates. One plate contained antibiotics to selected only for the gap editor, sgRNA, and repair template (typically chloramphenicol and ampicillin) and the other plate also included either rifampicin or kanamycin to select for edited cells. The next day colonies were counted. Genome editing efficiency was tabulated as being the number of colonies on the plates with rifampicin or kanamycin divided by the number of colonies on plates without rifampicin or kanamycin.
The measurement of gap editor toxicity in
Measurement of ssDNA-templated gap editing in E. coli by rifampicin resistance was performed by first co-transforming the strand annealing beta recombinase plasmid and a DNA modifying domain fused to a DNA binding domain such as Cas9. The resulting clones were inoculated into LB, antibiotics, and anhydrotetracycline for induction of beta recombinase expression. These cultures were prepared for electroporation and transformed with the sgRNA plasmid, and cultured for 3 hours in a rich media at 37° C. and shaking at 250 RPM prior to spot plating on two separate LB agar plates. One plate contained antibiotics to selected only for the gap editor, sgRNA, and recombinase. The other plate additionally included rifampicin to select for edited cells. The next day colonies were counted. Genome editing efficiency was tabulated as being the number of colonies on the plates with rifampicin divided by the number of colonies on plates without rifampicin.
It will be readily apparent to those skilled in the art that other suitable modifications and adaptations of the methods of the present disclosure described herein are readily applicable and appreciable, and may be made using suitable equivalents without departing from the scope of the present disclosure or the aspects and embodiments disclosed herein. Having now described the present disclosure in detail, the same will be more clearly understood by reference to the following examples, which are merely intended only to illustrate some aspects and embodiments of the disclosure, and should not be viewed as limiting to the scope of the disclosure. The disclosures of all journal references, U.S. patents, and publications referred to herein are hereby incorporated by reference in their entireties.
The present disclosure has multiple aspects, illustrated by the following non-limiting examples.
Example 1Experiments were conducted to assess the efficiency and toxicity of the gap editor complexes of the present disclosure. In one set of experiments, the DarT enzyme from E. coli EPEC with the attenuating mutation G49D was fused to the N-terminus of the fully or partially catalytically-dead version of ScCas9 (ScdCas9, or ScCas9 D10A also known as ScnCas9) with a long flexible linker. It was hypothesized that if chemical modification would occur, they would be made to the non-target strand exposed by ScdCas9 binding to its DNA target. Previous work indicated that DarT modifies thymine within a sequence motif possibly as wide as TYTN. Accordingly, genome editing in E. coli was assessed using these gap editor complexes.
The DarT-ScdCas9 fusion protein (gap editor complex) was targeted to four sites containing an NGG or NAG PAM and a TTTC motif on the non-target strand. The four sites surrounded a premature stop codon in the lacZ gene, which was the desired site of genome modification. The targets were chosen such that if a replication blocking lesion was introduced, a DNA gap would form that overlapped the premature stop codon. The four sites included two lagging strand targets and two leading strand targets. A plasmid encoding an arabinose inducible DarT-ScdCas9 was co-transformed with a plasmid containing a 1.5 kb repair template encoding mutations to block ScdCas9 re-targeting while repairing the lacZ stop codon. After culturing these colonies overnight, the cells were back-diluted into inducing medium, cultured for 8 hours, and then plated onto selective media with the β-galactosidase (lacZ gene product) indicator dye X-gal with the inducer IPTG.
When targeting only one site, the lacZ gene was efficiently repaired, as demonstrated by the results of in
Because a single replication block was being introduced into the DNA, it was expected that the dominant repair template would be the sister chromatid and not an ectopic repair template. Previous work has demonstrated that targeting two sites on either side of a DNA sequence-of-interest can boost genome modification, possibly by creating overlapping DNA gaps and interfering with sister chromatid repair. Therefore, it was hypothesized that the combination of DNA nicking and DNA modification/gap formation might similarly prevent sister chromatid repair, leaving the plasmid repair template as the preferred template for repair.
Cas9 nicking can drive low rates of genome editing in prokaryotes and eukaryotes. These nicks form single-ended double-strand breaks (seDSB) when encountered by the replisome. This typically involves replisome dissociation. These single-ended breaks are repaired by homologous recombination, most frequently with the sister chromatid. Importantly, in eukaryotic cells, Cas9 nicking can generate precise edits while minimizing indels presumably caused by non-homologous end-joining (NHEJ) machinery. There is no natural end joining partner at seDSBs, so NHEJ is inhibited at these breaks.
In accordance with the embodiments of the present disclosure, it was hypothesized that an overlapping DNA gap and seDSB could mutually exclude sister chromatid repair (e.g., exert synergistic effects). Where the seDSB end would typically look for homology on the sister chromatid, there would instead be a ssDNA gap. Similarly, where the DNA gap would typically find a homologous DNA template, there would be a seDSB, possibly resected to ssDNA. Therefore, the H848A mutation in ScdCas9 was re-activated, creating the target-strand nickase ScnCas9.
This nicking DarT-ScnCas9 fusion was tested in the lacZ repair assay described above using the most efficient target. As shown in
Experiments were also conducted to investigate the use of DarT's antitoxin partner, DarG, to determine whether it would eliminate the genome modification capacity of GE2. The N-terminal domain of DarG contains a glycohydrolase which can directly repair ADPr modified thymine. The C-terminal domain of DarG contains a DarT inhibitor. GE2 and GE2n were each co-expressed with full length DarG, the C-terminal domain of DarG, or the N-terminal domain of DarG in an operon in the lacZ gene repair assay (
Additionally, as would be recognized by one of ordinary skill in the art based on the present disclosure, either the N-terminal or C-terminal domains of DarG can be used to counteract DarT activity. The N-terminal domain can remove ADP ribose, reverting the nucleotide to its original state. The C-terminal domain can directly inhibit DarT activity. Thus, single domains of DarG can be expressed at a low level, and in some cases, randomly distributed through the cell, to help counteract off-target effects of the DarT-Cas protein. In some embodiments, a single DarT domain can be used to reduce off-target effects without affecting on-target genome modification activity.
Example 3Experiments were conducted to test the ability of a gap editing complex comprising a Scabin DNA-modifying domain in combination with a Cas9 DNA-recognition domain (Scabin-K130A-ScdCas9) to induce successful genome modification, measured based on the frequency of kanamycin gene repair in E. coli. In this exemplary set of experiments, expression of a Scabin-dCas9 fusion protein increased the frequency of kanamycin gene repair dependent on Scabin's DNA modification catalytic activity. Scabin is known to modify guanine within single and double-stranded DNA with an adenosine diphosphate ribose group, but it is structurally and evolutionarily divergent from DarT outside of a single shared catalytic motif. Recombination between the plasmid repair template and the targeted defective kanamycin gene in the E. coli genome results in repair of the targeted gene, and consequently, kanamycin resistance. Therefore, the fraction of kanamycin resistance serves as a readout for the rate of genome modification. The K130A mutation in Scabin attenuated Scabin's activity, which is otherwise toxic to the cells. The E160A mutation catalytically inactivates Scabin, removing all DNA modification activity (negative control). As shown in
In another set of exemplary experiments, the ability of a gap editing complex comprising a Mom DNA-modifying domain in combination with a Cas9 DNA-recognition domain (Mom-D149A-ScdCas9) to induce successful genome modification, measured based on the frequency of kanamycin gene repair in E. coli, was also tested. Fusion of the Mom to dCas9 and targeting a defective kanamycin gene resulted in recombination, genome modification, and thereby kanamycin resistant cells. The Mom protein is known to modify adenine with a methylcarbamoyl group, which is known to block DNA replication, triggering gap repair recombination. The D149A mutation in Mom attenuated the catalytic activity, which is otherwise lethal to the cells. As shown in
Experiments were also conducted to assess the DNA-modifying domain in the gap editing complexes of the present disclosure. Firstly,
Additionally, experiments were conducted to investigate whether DarT could be improved by reducing its toxic effects on cells. As shown in
Thus, these results demonstrate the novel CRISPR-based genome modification technology of the present disclosure, which facilitates efficient site-specific genome modification while minimizing the unintended modification and cellular toxicity associated with current genome editing approaches.
Example 5As shown in
As shown in
As shown in
As shown in
As shown in
DarT catalytic domain motif: X1X2X3X3 R (SEQ ID NO: 18), wherein X1 is L, I, V, or A; X2 is I, Q, K, T, or N; and X3 is any amino acid (
DarT catalytic domain motif: X1X1X1X1X2X3X4X5X6PFYFX7X1X1X8X9MX10X1 (SEQ ID NO: 19), wherein X1 is any amino acid; X2 is L, V, or I; X3 is H, G, N, S, or A; X4 is D or E; X5 is Y or F; X6 is V, I, or A; X7 is T, A, G, K, N, or W; X8 is S, T, N, M, or K; and X9 is P, V, M, I, A; X10 is L, M or F (
DarT catalytic domain motif: X1X2X3X4X5X6X7X8 (SEQ ID NO: 20), wherein X1 is F, Y, W, V, or C; X2 is V, L, I, A, C, or F; X3 is F, Y, or A; X4 is T, S, Y, or F; X5 is D, N, or S; X6 is G, R, S, A, M or Q; X7 is H, N, S, or Q; and X8 is A, G, C, H or K (
DarT catalytic domain motif: X1X2X3X4X5X6X7X8X9 (SEQ ID NO: 21), wherein X1 is and amino acid; X2 is R, K, H, E, F, L, T, or M; X3 is Y, R, K, D, E, or H; X4 is Q, M, E, Y, A, R, or H; X5 is A Q, S, or Y; X6 is E, A, or Q; X7 is F, A, L, E, V, or C; X8 is L, A, E, or M; and X9 is V, I, L, or A (
Scabin catalytic domain motif: X1X1X1X1X2X1EX3X4X5X6GGX7 (SEQ ID NO: 22), wherein X1 is and amino acid; X2 is Q, E, or R; X3 is V or I; X4 is A, L, V, S, or T; X5 is F, I, V, or L; X6 is P, A, or I; and X7 is I, V, or L (
Scabin catalytic domain motif: X1X2X3X4X5X6X7 (SEQ ID NO: 23), wherein X1 is S, T, or G; X2 is any amino acid; X3 is F, Y, or L; X4 is V, I, A, or L; X5 is S, G, or A; X6 is T or A; and X7 is T, S, or A (
Scabin catalytic domain motif: X1X2X3X2X4X2X5 (SEQ ID NO: 24), wherein X1 is L or V; X2 is any amino acid; X3 is R, H, or K; X4 is D, S, or A; and X5 is R or D (
Mom catalytic domain motif: X1HYX2X3 (SEQ ID NO: 25), wherein X1 is any amino acid; X2 is S or L; and X3 is H, G, K, R, N, D, or A (
Mom catalytic domain motif: EX1X2X3X4X5X6X7X8X7X9X10X11X12X13EX14 (SEQ ID NO: 26), wherein X1 is L, I, or F; X2 is N, G, S, or T; X3 is R or K; X4 is M, L, or A; X5 is W, A, C, V, F, or Y; X6 is L, I, F, M, V, C, or T; X7 is any amino acid; X8 is D or E; X9 is L A M, C, V, Q, or T; X10 is P, G, A, or L; X11 is R, K, H, T, or M; X12 is N or F; X13 is S, A, T, or G; and X14 is S or T (
Mom catalytic domain motif: X1X2DX3X4X4X5X4X4GX6X7YX8AX9X10X (SEQ ID NO: 27), wherein X1 is F, W, Y, or M; X2 is A or S; X3 is E, G, P, A, or T; X4 is any amino acid; X5 is G, C, or Q; X6 is T, V, Y, or I; X7 is V or I; X8 is Q, K, or R; X9 is A, S, C, T, or N; X10 is N, G, or A; X11 is F, W, or Y (
It is understood that the foregoing detailed description and accompanying examples are merely illustrative and are not to be taken as limitations upon the scope of the disclosure, which is defined solely by the appended claims and their equivalents.
All publications and patents mentioned in the above specification are herein incorporated by reference as if expressly set forth herein. Various changes and modifications to the disclosed embodiments will be apparent to those skilled in the art and may be made without departing from the spirit and scope thereof.
Claims
1. A composition for targeted genome modification, the composition comprising a gap editor complex comprising a DNA-recognition domain and a DNA-modifying domain, wherein the DNA-recognition domain binds a DNA target sequence in the genome, and wherein the DNA-modifying domain induces formation of a replication blocking moiety on at least one nucleotide in the genome.
2. The composition of claim 1, wherein the composition further comprises a donor nucleic acid template.
3. The composition of claim 1 or claim 2, wherein the donor nucleic acid template comprises a polynucleotide from an endogenous homologous sequence corresponding to the DNA target sequence.
4. The composition of claim 2, wherein the donor nucleic acid template comprise an exogenous single-stranded DNA (ssDNA) molecule, a double-stranded DNA (dsDNA) molecule, or an RNA molecule.
5. The composition of any of claims 2 to 4, wherein the presence of the donor nucleic acid template facilitates homology-directed gap repair and/or recombination, wherein the donor nucleic acid template or a fragment thereof is recombined into the genome of the DNA target sequence.
6. The composition of any of claims 1 to 5, wherein the composition comprises at least one guide RNA molecule.
7. The composition of any of claims 1 to 6, wherein the DNA-recognition domain comprises at least one Cas protein or fragment thereof lacking deoxyribonuclease activity.
8. The composition of any of claims 1 to 6, wherein the DNA-recognition domain comprises a complex of Cas proteins lacking deoxyribonuclease activity.
9. The composition of any of claims 1 to 6, wherein the DNA-recognition domain comprises a Cas protein or fragment thereof having nickase activity.
10. The composition of any of claims 1 to 9, wherein the Cas protein or Cas protein complex comprises a Type I Cascade, a Type II Cas9, a Type IV effector module, a Type V Cas12, a Cas9-related IscB, a Cas9-related TnpB, and combinations thereof.
11. The composition of any of claims 1 to 10, wherein the DNA-recognition domain and the DNA-modifying domain are functionally coupled.
12. The composition of claim 11, wherein functionally coupled comprises polypeptide fusions, peptide tags, peptide linkers, RNA tags, and any combinations thereof.
13. The composition of any of claims 1 to 12, wherein the DNA-modifying domain blocks DNA replication by adding the replication blocking moiety to:
- (i) at least one nucleotide in the DNA strand complementary to the DNA target sequence;
- (ii) at least one nucleotide in the DNA strand containing the DNA target sequence; or
- (iii) both at least one nucleotide in the DNA strand complementary to the DNA target sequence and at least one nucleotide in the DNA strand containing the DNA target sequence.
14. The composition of any of claims 1 to 13, wherein the DNA-recognition domain induces a single-stranded break in the DNA target strand, and wherein the DNA-modifying domain adds the replication blocking moiety to at least one nucleotide in the DNA strand complementary to the DNA target sequence.
15. The composition of any of claims 1 to 14, wherein the DNA-modifying domain has been engineered to have reduced DNA binding, increased specificity to single-stranded DNA, and/or decreased enzymatic activity.
16. The composition of any of claims 1 to 15, wherein the DNA-modifying domain catalyzes addition of ADP ribose to a thymine or guanine nucleotide.
17. The composition of any of claims 1 to 16, wherein the DNA-modifying domain comprises a DarT enzyme or a functional fragment, derivative, or variant thereof.
18. The composition of claim 16 or claim 17, wherein the DNA-modifying domain comprises a catalytic domain having at least 70% amino acid sequence identity with any of SEQ ID NOs: 18-21.
19. The composition of claim 17 or claim 18, wherein the DarT enzyme comprises one or more of the following amino acid substitutions: G49D, K56A, M86L, R92A, and/or R193A.
20. The composition of any of claims 1 to 16, wherein the DNA-modifying domain comprises a Scabin enzyme or a functional fragment, derivative, or variant thereof.
21. The composition of claim 16 or 20, wherein the DNA-modifying domain comprises a catalytic domain having at least 70% amino acid sequence identity with any of SEQ ID NOs: 22-24.
22. The composition of claim 20 or claim 21, wherein the Scabin enzyme comprises an amino acid substitution that is K130A.
23. The composition of any of claims 1 to 15, wherein the DNA-modifying domain catalyzes methylcarbamoylation of an adenine nucleotide.
24. The composition of claim 23, wherein the DNA-modifying domain comprises a Mom enzyme or a functional fragment, derivative, or variant thereof.
25. The composition of claim 23 or claim 24, wherein the DNA-modifying domain comprises a catalytic domain having at least 70% amino acid sequence identity with SEQ ID NO: 25-27.
26. The composition of claim 24 or claim 25, wherein the Mom enzyme comprises an amino acid substitution that is D149A.
27. The composition of any of claims 1 to 14, wherein the DNA-modifying domain catalyzes addition a replication blocking moiety selected from the group consisting of:
- glucose, threonyl carbamoyl adenosine, acetate, glyceryl, L-ascorbic acid, uridine, adenosine mono-phosphate, a lipid, an amino acid, agmatine, L-threonylcarbamoyladenylate, L-threonylcarbamoyl, methylthiolate, sulfur, a methyl group, S-adenosyl-L-methione or a subgroup of S-adenosyl-L-methione, and dimethylallyl diphosphate or a subgroup thereof.
28. The composition of any of claims 1 to 14, wherein the DNA-modifying enzyme domain comprises an enzyme or functional fragment, derivative, or variant thereof, selected from the group consisting of: Pierisin, Scabin, Cell cycle and apoptosis regulator 1 (CARP-1), SCO5461 protein (ScARP), adenine modification enzyme, acetyltransferase, amino acid transferase, nucleotidyl transferase, uridyltransferase, acyltransferase, ADP-ribsoyltransferase, methylthiotransferase, N-acetyl transferase 10, tRNA(Met) cytidine acetyltransferase (TmcA), tRNA cytidine acetyltransferase, GCN5-related N-acetyltransferase, lysidine synthase, m7G methyltransferase, N6 carbamoylmethyltransferase (Mom), N6-adenosine threonylcarbamoyltransferase, threonyl carbomyl transferase or threonyl carbomyl transferase complex, TsaB-TsaE-TsaD (TsaBDE) complex, tRNA N6-adenosine threonylcarbamoyltransferase (Qri7, Tcs4), methyltransferase, ATrm5a, tRNA:m1G/imG2 methyltransferase, tRNA (adenosine(37)-N6)-dimethylallyltransferase, tRNA dimethylallyltransferase (MiaA), and isopentenyltransferase.
29. The composition of any of claims 6 to 28, wherein the at least one guide RNA comprises gRNA, sgRNA, crRNA, or any combinations thereof.
30. The composition of any of claims 6 to 29, wherein the at least one guide RNA comprises a handle sequence and a targeting sequence.
31. The composition of claim 30, wherein the targeting sequence in the at least one guide RNA is complementary to the DNA target sequence.
32. The composition of any of claims 1 to 31, wherein the composition further comprises at least one gap editor accessory factor.
33. The composition of claim 32, wherein the at least one gap editor accessory factor comprises a protein that augments at least one step in a genome modification process.
34. The composition of claim 32, wherein the at least one gap editor accessory factor is recruited to the gap editor complex via interaction with the DNA-modifying domain, the DNA-recognition domain, and/or the at least one guide RNA.
35. The composition of claim 34, wherein the recruitment of the at least one gap editor accessory factor to the gap editor complex comprises a peptide tag, a peptide linker, an RNA tag, and any combinations thereof.
36. The composition of claim 32, wherein the at least one gap editor accessory factor comprises Rap, DarG, Orf, ExoI, Exonuclease III, PrimPol, RecJ, RecQ1, Rad51, Rad52, CtIP, Rad18, and any combinations thereof.
37. A kit for targeted genome modification, the kit comprising:
- a gap editor complex comprising a DNA-recognition domain and a DNA-modifying domain, wherein the DNA-recognition domain binds a DNA target sequence in the genome, and wherein the DNA-modifying domain induces formation of a replication blocking moiety on at least one nucleotide in the genome.
38. The kit of claim 37, wherein the kit further comprises a donor nucleic acid template.
39. The kit of claim 38, wherein the presence of the donor nucleic acid template facilitates homology-directed gap repair and/or recombination.
40. The kit of claim 37, wherein the kit further comprises a guide RNA molecule.
41. The kit of any of claims 37 to 40, wherein the DNA-recognition domain comprises at least one Cas protein or fragment thereof lacking deoxyribonuclease activity.
42. The kit of any of claims 37 to 41, wherein the DNA-recognition domain comprises at least one Cas protein or fragment thereof having nickase activity.
43. The kit of any of claims 37 to 42, wherein the Cas protein or Cas protein complex comprises a Type I Cascade, a Type II Cas9, a Type IV effector module, a Type V Cas12, a Cas9-related IscB, a Cas9-related TnpB, and combinations thereof.
44. The kit of any of claims 37 to 43, wherein the DNA-recognition domain and the DNA-modifying domain are functionally coupled.
45. The kit of any of claims 37 to 44, wherein the DNA-recognition domain induces a single-stranded break in the DNA target strand, and wherein the DNA-modifying domain adds the replication blocking moiety to at least one nucleotide in the DNA strand complementary to the DNA target sequence.
46. The kit of any of claims 37 to 45, wherein the DNA-modifying domain catalyzes addition of ADP ribose to a thymine or guanine nucleotide.
47. The kit of claim 46, wherein the DNA-modifying domain comprises a DarT enzyme, a Scabin enzyme, or a functional fragment, derivative, or variant thereof.
48. The kit of claim 47, wherein the DarT enzyme has been engineered to have reduced DNA binding, increased specificity to single-stranded DNA, and/or decreased enzymatic activity.
49. The kit of any of claims 37 to 48, wherein the DNA-modifying domain catalyzes addition a replication blocking moiety selected from the group consisting of: glucose, threonyl carbamoyl adenosine, acetate, glyceryl, L-ascorbic acid, uridine, adenosine mono-phosphate, a lipid, an amino acid, agmatine, L-threonylcarbamoyladenylate, L-threonylcarbamoyl, methylthiolate, sulfur, a methyl group, S-adenosyl-L-methione or a subgroup of S-adenosyl-L-methione, and dimethylallyl diphosphate or a subgroup thereof.
50. The kit of any of claims 37 to 49, wherein the DNA-modifying enzyme domain comprises an enzyme or functional fragment, derivative, or variant thereof, selected from the group consisting of: Pierisin, Scabin, Cell cycle and apoptosis regulator 1 (CARP-1), SCO5461 protein (ScARP), adenine modification enzyme, acetyltransferase, amino acid transferase, nucleotidyl transferase, uridyltransferase, acyltransferase, ADP-ribsoyltransferase, methylthiotransferase, N-acetyl transferase 10, tRNA(Met) cytidine acetyltransferase (TmcA), tRNA cytidine acetyltransferase, GCNS-related N-acetyltransferase, lysidine synthase, m7G methyltransferase, N6 carbamoylmethyltransferase (Mom), N6-adenosine threonylcarbamoyltransferase, threonyl carbomyl transferase or threonyl carbomyl transferase complex, TsaB-TsaE-TsaD (TsaBDE) complex, tRNA N6-adenosine threonylcarbamoyltransferase (Qri7, Tcs4), methyltransferase, ATrm5a, tRNA:m1G/imG2 methyltransferase, tRNA (adenosine(37)-N6)-dimethylallyltransferase, tRNA dimethylallyltransferase (MiaA), and isopentenyltransferase.
51. The kit of any of claims 40 to 50, wherein the at least one guide RNA comprises gRNA, sgRNA, crRNA, or any combinations thereof.
52. The kit of any of claims 40 to 51, wherein the at least one guide RNA comprises a handle sequence and a targeting sequence.
53. The kit of claim 52, wherein the targeting sequence in the at least one guide RNA is complementary to the DNA target sequence.
54. The kit of any of claims 37 to 53, wherein the kit further comprises at least one gap editor accessory factor.
55. A method for targeted genome modification, the method comprising:
- introducing any of the compositions of claims 1 to 36 into a cell; and
- assessing the cell for presence of a desired genome alteration.
56. The method of claim 55, wherein the gap editor complex and/or the at least one guide RNA molecule are introduced into the cell as a polypeptide(s), mRNA(s), and/or DNA expression construct(s).
57. The method of claim 55 or 56, wherein the gap editor complex and/or the guide RNA are introduced into the cell as part of a gene drive system.
58. The method of claim 55, wherein the cell is a prokaryotic cell or a eukaryotic cell.
59. The method of claim 55, wherein the cell is a mammalian cell.
60. The method of claim 55, wherein the cell is a plant cell.
61. The method of any of claims 47 to 60, wherein the method leads to a reduced degree of indel formation, chromosomal rearrangements, and/or DNA duplications.
62. The method of any of claims 47 to 61, wherein cell viability is enhanced and/or cell toxicity is reduced.
Type: Application
Filed: Feb 14, 2022
Publication Date: Apr 25, 2024
Inventors: Chase Lawrence Beisel (Raleigh, NC), Scott Patrick Collins (Raleigh, NC)
Application Number: 18/546,378
